Djukanovic, Stefana et al. published their research in Industrial Crops and Products in 2020 | CAS: 109-17-1

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Computed Properties of C16H26O7

Antistaphylococcal and biofilm inhibitory activities of Frangula alnus bark ethyl-acetate extract was written by Djukanovic, Stefana;Cvetkovic, Stefana;Loncarevic, Branka;Ljesevic, Marija;Nikolic, Biljana;Simin, Natasa;Bekvalac, Kristina;Kekic, Dusan;Mitic-Culafic, Dragana. And the article was included in Industrial Crops and Products in 2020.Computed Properties of C16H26O7 This article mentions the following:

Since that we are facing with a serious problem of bacterial resistance it is necessary to find a new antibacterial agents in fight with it. Frangula alnus is traditionally used plant but its antibiofilm potential is poorly investigated. The aim of the study was to investigate antibiofilm activity of F. alnus ethyl-acetate extract (FA) toward S. aureus ATCC strains and clin. isolates as well as its influence on respiration in planktonic and biofilm form. The qual. GCxGC-MS and quant. LC-MS/MS anal. revealed that FA extract was rich in phenols and flavonoids and emodin, chatechin, and ester 4-ethoxy benzoic acid were the most dominant components. Results obtained through microdillution assay showed that FA possesses strong antibacterial activity. Furthermore, crystal violet staining of biofilm biomass demonstrated that extract had strong effect on biofilm formation of all tested strains while effect on preformed biofilms was less pronounced. The effect on biofilm was confirmed with SEM where the changes in biofilm structure were noticed. The activity of extract on the consumption of O2 and production of CO2 was monitored using the Micro-Oxymax respirometer. Interestingly, respiration of the most strains was decreased in planktonic form as well as in biofilms. Results obtained in this study are a good basis for further research in order to discover the mechanism of action of the FA extract on connection between biofilm and respiration. In the experiment, the researchers used many compounds, for example, ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1Computed Properties of C16H26O7).

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Computed Properties of C16H26O7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tateno, Kotaro et al. published their research in Chemistry – A European Journal in 2019 | CAS: 1214264-88-6

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine (cas: 1214264-88-6) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Related Products of 1214264-88-6

Fluorescent Short-Stranded Helical Foldamers Based on L-shaped Dibenzopyrrolo[1,2-a][1,8]naphthyridine was written by Tateno, Kotaro;Ono, Kosuke;Kawai, Hidetoshi. And the article was included in Chemistry – A European Journal in 2019.Related Products of 1214264-88-6 This article mentions the following:

Helical structures were constructed by using 蟺-spacer-bridged dimers of dibenzopyrrolo[1,2-a][1,8]naphthyridine, which has a highly fluorescent L-shaped 蟺-extended skeleton. Three dimers with biphenylene , phenanthrene , and m-phenylene spacers, as well as a fixed-helical dimer where two quinolone rings were covalently crosslinked, were designed and prepared 1H NMR and ROESY spectra revealed that dimers adopted helical forms in solution, whereas m-phenylene dimer did not. The helical conformation of phenanthrene dimer was strengthened by addition of either polar or nonpolar solvents to the chloroform solution, which suggested that 蟺-蟺 stacking was the main contributor to the stabilization of the helical structure. All of the dimers, including fixed-helical dimer , emitted fluorescence with high quantum yields (蠁=0.79-0.86). In the experiment, the researchers used many compounds, for example, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine (cas: 1214264-88-6Related Products of 1214264-88-6).

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine (cas: 1214264-88-6) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Related Products of 1214264-88-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Sivak, Ivan et al. published their research in Journal of Organic Chemistry in 2018 | CAS: 5856-63-3

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Reference of 5856-63-3

Stereoselective synthesis of functionalized 伪-amino acids isolated by filtration was written by Sivak, Ivan;Toberny, Michal;Kyselicova, Andrea;Caletkova, Ol’ga;Berkes, Dusan;Jakubec, Pavol;Kolarovic, Andrej. And the article was included in Journal of Organic Chemistry in 2018.Reference of 5856-63-3 This article mentions the following:

Crystallization-induced diastereomer transformation (CIDT) represents a highly appealing and convenient synthetic tool. Despite its numerous advantages, it remains rather rarely used due to its uncertain predictability to occur. Herein, we describe CIDT based on aza-Michael reactions of diversely functionalized (E)-3-acylacrylic acids. This method provides direct access to a broad variety of 伪-amino acid derivatives in excellent stereochem. purities. In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Reference of 5856-63-3).

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Reference of 5856-63-3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kondoh, Azusa et al. published their research in Chemistry – A European Journal in 2022 | CAS: 873-76-7

(4-Chlorophenyl)methanol (cas: 873-76-7) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Quality Control of (4-Chlorophenyl)methanol

Synthesis of 2,2-Disubstituted 2H-Chromenes through Carbon-Carbon Bond Formation Utilizing a [1,2]-Phospha-Brook Rearrangement under Broensted Base Catalysis was written by Kondoh, Azusa;Terada, Masahiro. And the article was included in Chemistry – A European Journal in 2022.Quality Control of (4-Chlorophenyl)methanol This article mentions the following:

A new methodol. for the synthesis of 2,2-disubstituted 2H-chromenes was developed by utilizing the [1,2]-phospha-Brook rearrangement under Broensted base catalysis. Phosphazene P2-tBu efficiently catalyzed the addition reaction of 4H-chromen-4-ols containing a diethoxyphosphoryl group with 伪,尾-unsaturated ketones, which involved the catalytic generation of a carbanion through the [1,2]-phospha-Brook rearrangement and subsequent conjugate addition at the 2-position to afford adducts possessing an alkenylphosphate moiety in a highly diastereoselective manner. Further transformation of the adducts based on a nickel-catalyzed cross-coupling reaction with arylzinc reagents provided densely functionalized 2,2-disubstituted 2H-chromenes. In the experiment, the researchers used many compounds, for example, (4-Chlorophenyl)methanol (cas: 873-76-7Quality Control of (4-Chlorophenyl)methanol).

(4-Chlorophenyl)methanol (cas: 873-76-7) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Quality Control of (4-Chlorophenyl)methanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zhang, Lang et al. published their research in Food Control in 2022 | CAS: 3391-86-4

Oct-1-en-3-ol (cas: 3391-86-4) belongs to alcohols. The oxygen atom of the strongly polarized O鈥旽 bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Quality Control of Oct-1-en-3-ol

Changes in flavor, heterocyclic aromatic amines, and quality characteristics of roasted chicken drumsticks at different processing stages was written by Zhang, Lang;Badar, Iftikhar Hussain;Chen, Qian;Xia, Xiufang;Liu, Qian;Kong, Baohua. And the article was included in Food Control in 2022.Quality Control of Oct-1-en-3-ol This article mentions the following:

This study evaluated changes in flavor, heterocyclic aromatic amines (HAAs), and quality characteristics of roasted chicken drumsticks at three different processing stages: marinating (MS), low-temperature roasting (LRS), and high-temperature roasting (HRS). Raw chicken drumsticks (RC) served as the control. Water content and L-value were significantly highest (P < 0.05), whereas a-value and b-value were significantly lowest (P < 0.05) in the HRS sample. Furthermore, the HRS sample had a significantly higher (P < 0.05) pH value than the RC, MS, and LRS samples. A total of 48 different volatile compounds were detected and electronic nose results indicated similar odor profiles between the MS and LRS samples. The LRS and HRS samples had significantly higher (P < 0.05) contents of PhIP, Harman, and Norharman than the RC and MS samples, which can be explained by the higher contents of precursors phenylalanine, tryptophan, and creatinine in the LRS and HRS samples compared to those in the RC and MS samples. Correlation anal. result indicated that the aldehydes and ketones are responsible for the PhIP, Harman, and Norharman formation. These results provide guidance for revealing the flavor and HAA formation of roasted chicken during processing. In the experiment, the researchers used many compounds, for example, Oct-1-en-3-ol (cas: 3391-86-4Quality Control of Oct-1-en-3-ol).

Oct-1-en-3-ol (cas: 3391-86-4) belongs to alcohols. The oxygen atom of the strongly polarized O鈥旽 bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Quality Control of Oct-1-en-3-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Li, Weili et al. published their research in LWT–Food Science and Technology in 2022 | CAS: 3391-86-4

Oct-1-en-3-ol (cas: 3391-86-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Quality Control of Oct-1-en-3-ol

Insight into the aroma dynamics of Dongpo pork dish throughout the production process using electronic nose and GCxGC-MS was written by Li, Weili;Zheng, Lanting;Xiao, Yue;Li, Liangchao;Wang, Ning;Che, Zhenming;Wu, Tao. And the article was included in LWT–Food Science and Technology in 2022.Quality Control of Oct-1-en-3-ol This article mentions the following:

In this study, the aroma dynamic changes throughout the manufacturing process of Dongpo pork dish (DPD) model were investigated with electronic nose and two-dimensional gas chromatog. coupled with mass spectrometry (GC x GC-MS). The results of both electronic nose and GC x GC-MS studies were consistent in that the frying and steaming stages had the greatest effect on the aroma composition of DPD. A total of 111 volatiles were detected, 59 of which were key volatiles. The odor activity analyses further revealed that pentanal, hexanal, 1-octen-3-ol, 2,3-pentanedione and (E)-2-octenal as key aroma contributors during the frying stage, while 3-methylbutyraldehyde were mainly formed during the steaming stage. These aromas were mainly generated through the thermal degradation of lipids and the Maillard reaction. Hence, this study, for the first time, provided some profound insights for the industrial production and flavor control of DPD products. In the experiment, the researchers used many compounds, for example, Oct-1-en-3-ol (cas: 3391-86-4Quality Control of Oct-1-en-3-ol).

Oct-1-en-3-ol (cas: 3391-86-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Quality Control of Oct-1-en-3-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Telfer, Shane G. et al. published their research in Angewandte Chemie, International Edition in 2004 | CAS: 1122-71-0

6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Recommanded Product: 1122-71-0

Noncovalent ligand strands for transition-metal helicates: The straightforward and stereoselective self-assembly of dinuclear double-stranded helicates using hydrogen bonding was written by Telfer, Shane G.;Sato, Tomohiro;Kuroda, Reiko. And the article was included in Angewandte Chemie, International Edition in 2004.Recommanded Product: 1122-71-0 This article mentions the following:

A genuinely supramol. approach to transition-metal helicates is presented in which eight simple components (four ions and four small mols.) self-assemble to form dinuclear double helicates, where the ligand strands are built up through hydrogen-bonding interactions. The complexes [Co2(L)2(L-H)2Cl2] (L = 6-methylpyridin-2-ylmethanol, R-1-(6-methylpyridin-2-yl)ethanol and (6-methylpyridin-2-yl)nitromethanol) self-assembled and were characterized by x-ray crystallog. The self-assembly process is highly stereoselective. In the experiment, the researchers used many compounds, for example, 6-Methyl-2-pyridinemethanol (cas: 1122-71-0Recommanded Product: 1122-71-0).

6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Recommanded Product: 1122-71-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Della Ca’, Nicola et al. published their research in Tetrahedron in 2015 | CAS: 60666-70-8

(2-Bromo-5-chlorophenyl)methanol (cas: 60666-70-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Safety of (2-Bromo-5-chlorophenyl)methanol

Formation of a carbonyl group ortho to a biaryl structure or a 6H-dibenzopyran by a palladium/norbornene-catalyzed ordered reaction sequence was written by Della Ca’, Nicola;Fontana, Marco;Xu, Di;Cremaschi, Mirko;Lucentini, Riccardo;Zhou, Zhi-Ming;Catellani, Marta;Motti, Elena. And the article was included in Tetrahedron in 2015.Safety of (2-Bromo-5-chlorophenyl)methanol This article mentions the following:

Developments are reported in the catalytic synthesis of biaryls containing an ortho-carbaldehyde or 6H-dibenzopyrans in the presence of palladium/norbornene as catalyst. The reaction of o-substituted aryl iodides and o-bromobenzyl alcs. proceeds by unsym. aryl-aryl coupling to form a seven-membered oxapalladacycle intermediate, which may undergo an intramol. redox process to form carbonyl groups or a C-O coupling to six-membered cyclic ethers. The predominant formation of dibenzopyrans as well as of biaryl structures containing the oxidized CHO group in one ring and the reduced CH2OH in the other is described along with some mechanistic insights. In the experiment, the researchers used many compounds, for example, (2-Bromo-5-chlorophenyl)methanol (cas: 60666-70-8Safety of (2-Bromo-5-chlorophenyl)methanol).

(2-Bromo-5-chlorophenyl)methanol (cas: 60666-70-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Safety of (2-Bromo-5-chlorophenyl)methanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Ranoo, Surojit et al. published their research in Journal of Molecular Liquids in 2022 | CAS: 111-46-6

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Application of 111-46-6

Tuning magnetic heating efficiency of colloidal dispersions of iron oxide nano-clusters by varying the surfactant concentration during solvothermal synthesis was written by Ranoo, Surojit;Lahiri, B. B.;Damodaran, Shima P.;Philip, John. And the article was included in Journal of Molecular Liquids in 2022.Application of 111-46-6 This article mentions the following:

Magnetic fluid hyperthermia (MFH) is being actively sought as a supplementary cancer therapy, where enhancing the MFH efficiency is essential for reducing dosage and field exposure. Owing to the superior magnetic properties, magnetic nano-clusters (MNCs) are being developed as MFH agents, where the role of synthesis routes, colloidal stability and magneto-structural properties on MFH efficiency requires further attention. In this article, we report the tuning of MFH efficiency of water and diethylene glycol-based magnetic nanofluids containing iron-oxide MNCs of sizes 鈭?125 to 539 nm, obtained by varying the surfactant concentration Magnetite MNCs are prepared via solvothermal route, where the primary nano-crystallite (MNP) size is varied from 7.4 卤 0.7 to 25.0 卤 0.8 nm by reducing the sodium citrate (surfactant) concentration from 29 to 0.29 mg/mL. With decreasing surfactant concentration, the amount of sodium citrate absorbed on the surface of the freshly formed nano-seeds reduces, which lowers the electrostatic stabilization in polar media and favors the growth of larger MNPs that results in comparatively larger MNCs. Transmission electron microscopy and at. force microscopy based studies indicate the monodisperse spherical morphol. of the MNCs, consisting of several primary nano-crystallites. Room temperature isothermal magnetization measurements indicate high saturation magnetization and superparamagnetic nature of the MNCs, which are beneficial for MFH applications. Magneto-calorimetry experiments are performed for the accurate estimation of the MFH efficiency of the colloidal dispersions of the MNCs. Exptl. findings indicate that the heating efficiency increases from 15.24 卤1.22 to 193.8 卤 5.2 W/gFe (i.e., an enhancement of 鈭?12.7 times), at a field exposure condition of 33.1 kA/m and 126 kHz, when the primary nano-crystallite size is increased by 鈭?3.4 times by reducing the surfactant concentration It is observed that the heating efficiency decreases linearly with the logarithm of surfactant concentration in all the cases, which is attributed to the variations in primary nano-crystallite sizes and the resultant magnetic losses. Magneto-calorimetric experiments, using MNCs immobilized in high viscosity agar matrix, indicate insignificant contributions from the whole-scale Brownian relaxation, and the heating efficiency is found to be solely dependent on the magnetic losses of the primary nano-crystallites. With increasing primary nano-crystallite size, augmentation of heating efficiency is due to the increase in magnetization and dynamic coercivity, which is confirmed from theor. calculations using the high frequency hysteresis loops and sweeping rate modified Stoner Wohlfarth model. The obtained results indicate the possibility of tuning hyperthermia efficiency of MNCs by varying the surfactant concentration, which is beneficial for designing colloidally stable dispersions of MNCs with improved MFH efficiency. In the experiment, the researchers used many compounds, for example, 2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6Application of 111-46-6).

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Application of 111-46-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tian, Hongyu et al. published their research in Industrial Crops and Products in 2022 | CAS: 111-46-6

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Computed Properties of C4H10O3

Self-healing modified liquefied lignocellulosic cross-linked bio-based polymer for controlled-release urea was written by Tian, Hongyu;Zhang, Lina;Sun, Xiao;Cui, Jing;Dong, Jingjing;Wu, Liang;Wang, Yanfeng;Wang, Lingli;Zhang, Min;Liu, Zhiguang;Lu, Panfang. And the article was included in Industrial Crops and Products in 2022.Computed Properties of C4H10O3 This article mentions the following:

Alkali-hydrolyzed lignocellulose was liquefied into polyols by acid-catalyzed dissolution, and then cross-linked with castor oil to prepare bio-based cross-linked polyurethane. Then, bis (2-hydroxyethyl) disulfide (SS) with self-healing function was used to reduce foaming in the curing process of polyurethane coating. Afterwards, disulfide bond modified crosslinked bio-based polyurethane coating (BCSPU) was applied to controlled-release urea (CRU). The results of excitation-emission matrixes indicated that SS made the coating smoother and denser and preventing the release of non-film-forming substances. Crosslinking modification technol. significantly extended the controlled release longevity of CRU by 77.3%, and the self-healing modification further prolonged the nitrogen release longevity by 61.5%. In addition, modified coating materials were non-toxic to wheat seeds and easily biodegradable in the soil. Crosslinking, self-healing modified controlled-release urea has enormous application potential in sustainable agriculture. In the experiment, the researchers used many compounds, for example, 2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6Computed Properties of C4H10O3).

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Computed Properties of C4H10O3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts