Wang, Runping et al. published their research in Angewandte Chemie, International Edition in 2021 | CAS: 142253-56-3

1-Boc-Azetidine-3-yl-methanol (cas: 142253-56-3) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Name: 1-Boc-Azetidine-3-yl-methanol

O2-Assisted Four-Component Reaction of Vinyl Magnesium Bromide with Chiral N-tert-Butanesulfinyl Imines To Form syn-1,3-Amino Alcohols was written by Wang, Runping;Luo, Jingfan;Zheng, Chunmei;Zhang, Hongyun;Gao, Lu;Song, Zhenlei. And the article was included in Angewandte Chemie, International Edition in 2021.Name: 1-Boc-Azetidine-3-yl-methanol This article mentions the following:

An O2-assisted, four-component reaction has been developed to synthesize a wide range of syn-1,3-amino alcs. in one step. The reaction proceeds by oxygenation of vinyl magnesium bromide (component-I) with O2 (component-II) to give a magnesium enolate of acetaldehyde, which undergoes addition to a chiral N-tert-butanesulfinyl imine (component-III) followed by a sequential addition with excess vinyl magnesium bromide (component-IV). The approach allows diastereoselective synthesis of anti/syn- and syn/syn-3-amino-1,5-diols in good yields with high diastereoselectivity. The method was illustrated in an efficient, four-step synthesis of piperidine alkaloid (-)-2′-epi-ethylnorlobelol. In the experiment, the researchers used many compounds, for example, 1-Boc-Azetidine-3-yl-methanol (cas: 142253-56-3Name: 1-Boc-Azetidine-3-yl-methanol).

1-Boc-Azetidine-3-yl-methanol (cas: 142253-56-3) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Name: 1-Boc-Azetidine-3-yl-methanol

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Alcohol – Wikipedia,
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Pavlyuchenko, A. I. et al. published their research in Zhurnal Organicheskoi Khimii in 1976 | CAS: 15777-70-5

4-Hydroxy-3-methylbenzonitrile (cas: 15777-70-5) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). 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.SDS of cas: 15777-70-5

Liquid-crystal compounds. VIII. Methyl-substituted p-alkyl- and p-alkoxycinnamic acids and their cyanophenyl esters was written by Pavlyuchenko, A. I.;Smirnova, N. I.;Kovshev, E. I.;Titov, V. V.. And the article was included in Zhurnal Organicheskoi Khimii in 1976.SDS of cas: 15777-70-5 This article mentions the following:

P-RC6H4CH:CMeCO2H (I; R = Bu, pentyl, hexyl) were prepared in 18.4-21.1% yield by reaction of RC6H4CHO with MeCHBrCO2Et followed by hydrolysis; their p-cyanophenyl esters were prepared by standard procedures. The p-RC6H4CMe:CHCO2H (II; R = Bu, pentyl, hexyl, heptyl, octyl) were prepared in 20.1-25.0% yield by condensation of p-RC6H4COMe with HOAc; their p-cyanophenyl esters were also prepared Six III (R = Bu, heptyl; R1 = 2- and 3-Me, H; R2 = 2- and 3-Me, H) were also prepared by standard methods. In I, II, and III the temperature of clearing was lowered and the mesomorphic interval narrowed with respect to the unsubstituted compounds II have a wider mesomorphic range than p-alkylcinnamic acids. In the experiment, the researchers used many compounds, for example, 4-Hydroxy-3-methylbenzonitrile (cas: 15777-70-5SDS of cas: 15777-70-5).

4-Hydroxy-3-methylbenzonitrile (cas: 15777-70-5) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). 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.SDS of cas: 15777-70-5

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Alcohol – Wikipedia,
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Mauerwerk, Marlise Teresinha et al. published their research in Aquaculture Research in 2022 | CAS: 137-08-6

Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate (cas: 137-08-6) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Product Details of 137-08-6

Biodiesel-derived glycerol as a dietary maize replacement for silver catfish (Rhamdia quelen) during the fattening phase was written by Mauerwerk, Marlise Teresinha;Zadinelo, Izabel Volkweis;Dias, Patricia da Silva;Balen, Rafael Ernesto;Bombardelli, Robie Allan;Meurer, Fabio. And the article was included in Aquaculture Research in 2022.Product Details of 137-08-6 This article mentions the following:

The aim of the present study was to assess the effects of crude biodiesel-derived glycerol on the zootech. performance, carcass and fillet chem. composition, and blood parameters of silver catfish (Rhamdia quelen) during the fattening phase. A total of 150 adult silver catfish specimens (mean weight 188.89 ± 0.60 g) were distributed in thirty 1000 L-tanks containing a water recirculation system with mech. filter and biofilter, in a completely randomized design comprising six treatments, 0%, 20%, 40%, 60%, 80% and 100% maize replacement by glycerol, with five repetitions each. The experiment was conducted for 206 days. Silver catfish morphometric parameters were not influenced (p > 0.05) by the glycerol maize replacement, although silver catfish standard length and width exhibited linear improvements (p < 0.05) with the dietary glycerol replacement. Fillet yield was affected (p < 0.05) by glycerol maize replacement, where the 80% replacement treatment led to better fillet yields (46.04%), differing only from the 20% replacement treatment (42.40% fillet yields). The blood plasma levels of glucose, pyruvic glutamic transaminase and triglycerides were influenced by the treatments (p < 0.05). The crude protein of fillet was influenced by the treatments (p < 0.05), where the highest value was observed in 100% glycerol maize replacement. Therefore, crude glycerol derived from biodiesel production is a suitable alternative energy source ingredient for silver catfish during their fattening phase, as it can replace maize in up to 100%. In the experiment, the researchers used many compounds, for example, Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate (cas: 137-08-6Product Details of 137-08-6).

Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate (cas: 137-08-6) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Product Details of 137-08-6

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Shang, Feng-Kang et al. published their research in ACS Physical Chemistry Au 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Product Details of 873-76-7

Nanoscale Assembly of CdS/BiVO4 Hybrids for Coupling Selective Fine Chemical Synthesis and Hydrogen Production under Visible Light was written by Shang, Feng-Kang;Qi, Ming-Yu;Tan, Chang-Long;Tang, Zi-Rong;Xu, Yi-Jun. And the article was included in ACS Physical Chemistry Au in 2022.Product Details of 873-76-7 This article mentions the following:

Simultaneously utilizing photogenerated electrons and holes in one photocatalytic system to synthesize value-added chems. and clean hydrogen (H2) energy meets the development requirements of green chem. Herein, we report a binary material of CdS/BiVO4 combining one-dimensional (1D) CdS nanorods (NRs) with two-dimensional (2D) BiVO4 nanosheets (NSs) constructed through a facile electrostatic self-assembly procedure for the selectively photocatalytic oxidation of aromatic alcs. integrated with H2 production, which exhibits significantly enhanced photocatalytic performance. Within 2 h, the conversion of aromatic alcs. over CdS/BiVO4-25 was approx. 9-fold and 40-fold higher than that over pure CdS and BiVO4, resp. The remarkably improved photoactivity of CdS/BiVO4 hybrids is mainly ascribed to the Z-scheme charge separation mechanism in the 1D/2D heterostructure derived from the interface contact between CdS and BiVO4, which not only facilitates the separation and transfer of charge carriers, but also maintains the strong reducibility of photogenerated electrons and strong oxidizability of photogenerated holes. It is anticipated that this work will further stimulate interest in the rational design of 1D/2D Z-scheme heterostructure photocatalysts for the selective fine chem. synthesis integrated with H2 evolution. In the experiment, the researchers used many compounds, for example, (4-Chlorophenyl)methanol (cas: 873-76-7Product Details of 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Product Details of 873-76-7

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Choudhary, Pushpa et al. published their research in Aquaculture Nutrition in 2022 | CAS: 137-08-6

Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate (cas: 137-08-6) 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. 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.Application In Synthesis of Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate

Effect of graded levels of dietary emamectin benzoate on immunity, enzyme activity, and withdrawal period in Labeo rohita juveniles (Hamilton, 1822) was written by Choudhary, Pushpa;Swain, Priyabrat;Das, Rakesh;Sahoo, Satya Narayan;Das, Krushna Chandra;Patil, Prasanna Kumar;Mishra, Sudhansu Sekhar. And the article was included in Aquaculture Nutrition in 2022.Application In Synthesis of Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate This article mentions the following:

This study was conducted to evaluate the effect of dietary emamectin benzoate (EB) levels on immune responses, serum enzyme activities, and retention of EB in muscle tissue to establish the withdrawal period in rohu, Labeo rohita juveniles (avg. weight 18 ± 0.11 g). To ascertain this, 450 healthy L. rohita juveniles were fed with EB in graded doses viz., at 50 (1x), 125 (2.5x), 250 (5x), and 375 (7.5x) μg kg-1 of fish biomass day-1, resp., in triplicate for 21 days through a basal feed. Upon completion of 21 days, the same exptl. fish were fed with basal feed (without EB) for another 14 days to measure the retention of EB in the muscle tissue. Each 7-day interval, five fish were randomly sampled. The results showed that respiratory burst activity, myeloperoxidase activity, bacterial hemagglutination, and haemolysis activities were improved significantly (p < 0.05) in 1x and 2.5x dose fed group from 7th day onwards until 14th day. Few selected enzyme activities viz., LDH and ALP were found to be significantly (p < 0.05) high in the fish fed with EB at 5x and 7.5x dose compared to 1x. The LC-MS/MS study of the exptl. fish discloses that EB was retained in muscle tissue at a dose-dependent manner and significantly (p < 0.05) lowest level (0.341 ± 0.03 ppb) was retained in the fish fed with 1x dose of EB. Hence, 1x dose of EB may be adhered to treat L. rohita juveniles through feed with 14 days of withdrawal period. In the experiment, the researchers used many compounds, for example, Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate (cas: 137-08-6Application In Synthesis of Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate).

Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate (cas: 137-08-6) 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. 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.Application In Synthesis of Calcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate

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Alcohol – Wikipedia,
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Tatiana, Nistor Manuela et al. published their research in Colloid and Polymer Science in 2018 | CAS: 4074-88-8

Diethyleneglycoldiacrylate (cas: 4074-88-8) 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. 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.Computed Properties of C10H14O5

Hybrid collagen/pNIPAAM hydrogel nanocomposites for tissue engineering application was written by Tatiana, Nistor Manuela;Cornelia, Vasile;Tatia, Rodica;Aurica, Chiriac. And the article was included in Colloid and Polymer Science in 2018.Computed Properties of C10H14O5 This article mentions the following:

The present work explores new hybrid bioactive, enzymically degradable hydrogel nanocomposites. They are composed by stimuli-sensitive semi-interpenetrating collagen/poly(N-iso-Pr acrylamide) polymeric matrix, Dellite 67G and Cloisite 93A nanoclays, and hydroxyapatite particles. Morphol. of the hybrid hydrogel nanocomposites was examined by near IR chem. imaging, X-ray diffraction, SEM, and transmission electron microscopy techniques. It has been found that the porous hydrogel nanocomposites showed a mix between intercalated and exfoliated structure, with interconnected pores and the inorganic material was evenly distributed in the polymeric matrix because of specific interactions between components. The collagen resistance against enzymic degradation and the thermal stability were improved due to the protein encapsulation in the synthetic polymer matrix. The hydrogel nanocomposites showed suitable swelling characteristics for tissue engineering. In vitro cytocompatibility and cell viability revealed that the hybrid nanocomposites were non-cytotoxic for rat osteoblasts. These hybrid nanocomposites were designed as potential synthetic bone tissue engineering. [Figure not available: see fulltext.]. In the experiment, the researchers used many compounds, for example, Diethyleneglycoldiacrylate (cas: 4074-88-8Computed Properties of C10H14O5).

Diethyleneglycoldiacrylate (cas: 4074-88-8) 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. 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.Computed Properties of C10H14O5

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Alcohol – Wikipedia,
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Zhang, Jun-Hui et al. published their research in Analytical Chemistry (Washington, DC, United States) in 2014 | CAS: 5856-63-3

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) 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. 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.Synthetic Route of C4H11NO

Novel Inorganic Mesoporous Material with Chiral Nematic Structure Derived from Nanocrystalline Cellulose for High-Resolution Gas Chromatographic Separations was written by Zhang, Jun-Hui;Xie, Sheng-Ming;Zhang, Mei;Zi, Min;He, Pin-Gang;Yuan, Li-Ming. And the article was included in Analytical Chemistry (Washington, DC, United States) in 2014.Synthetic Route of C4H11NO This article mentions the following:

Chiral nematic mesoporous silica (CNMS) has attracted widespread attention due to some unique features, such as its nematic structure, chirality, large pore size, high temperature resistance, low cost, and ease of preparation The authors 1st reported the use of CNMS as a stationary phase for capillary gas chromatog. (GC). The CNMS-coated capillary column not only gives good selectivity for the separation of linear alkanes, aromatic hydrocarbons, polycyclic aromatic hydrocarbons (PAHs), and isomers but also offers excellent enantioselectivity for chiral compounds Compared with enantioseparations on com. β-DEX 120 and Chirasil-L-Val columns, a CNMS-coated capillary column offers excellent enantioselectivity, chiral recognition complementarity, and the separation of analytes within short elution times. It can also be potentially applied in high-temperature GC at >350°. CNMS could soon become very attractive for separations In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Synthetic Route of C4H11NO).

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) 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. 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.Synthetic Route of C4H11NO

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Alcohol – Wikipedia,
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Ding, Ling et al. published their research in ChemSusChem in 2022 | CAS: 2216-51-5

(1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol (cas: 2216-51-5) belongs to alcohols. The oxygen atom of the strongly polarized O―H 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.SDS of cas: 2216-51-5

Visible Light-Induced Hydrosilylation of Electron-Deficient Alkenes by Iron Catalysis was written by Ding, Ling;Niu, Kaikai;Liu, Yuxiu;Wang, Qingmin. And the article was included in ChemSusChem in 2022.SDS of cas: 2216-51-5 This article mentions the following:

Regioselective photochem. hydrosilylation of activated alkenes R1CH:CR2(EWG) with Ph3SiH catalyzed by iron trichloride, afforded linear triphenylsilanes Ph3SiCHR1CHR2(EWG) (R1, R2 = H, Me, CF3, CO2Me; EWG = carboxylate, CN, CHO, CONHPh). Herein, we reported a method for iron-catalyzed, visible-light-induced hydrosilylation reactions of electron-deficient alkenes to produce value-added silicon compounds Alkenes bearing functional groups with different steric properties were suitable substrates, as were derivatives of structurally complex natural products. Mechanistic studies showed that chlorine radicals generated by iron-catalyzed ligand-to-metal charge transfer in the presence of lithium chloride promoted the formation of silyl radicals. In the experiment, the researchers used many compounds, for example, (1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol (cas: 2216-51-5SDS of cas: 2216-51-5).

(1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol (cas: 2216-51-5) belongs to alcohols. The oxygen atom of the strongly polarized O―H 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.SDS of cas: 2216-51-5

Referemce:
Alcohol – Wikipedia,
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Matt, Christof et al. published their research in Angewandte Chemie, International Edition in 2022 | CAS: 2216-51-5

(1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol (cas: 2216-51-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.SDS of cas: 2216-51-5

Catalytic Asymmetric β-Oxygen Elimination was written by Matt, Christof;Orthaber, Andreas;Streuff, Jan. And the article was included in Angewandte Chemie, International Edition in 2022.SDS of cas: 2216-51-5 This article mentions the following:

A catalytic enantioselective β-O-elimination reaction is reported in the form of a zirconium-catalyzed asym. opening of meso-ketene acetals. Furthermore, a regiodivergent β-O-elimination is demonstrated. The reaction proceeds under mild conditions, at low catalyst loadings, and produces chiral monoprotected cis-1,2-diols in good yield and enantiomeric excess. The combination with a Mitsunobu reaction or a one-pot hydroboration/Suzuki reaction sequence then gives access to addnl. diol and aminoalc. building blocks. A stereochem. anal. supported by DFT calculations reveals that a high selectivity in the hydrozirconation step is also important for achieving high enantioselectivity, although it does not constitute the asym. step. This insight is crucial for the future development of related asym. β-elimination reactions. In the experiment, the researchers used many compounds, for example, (1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol (cas: 2216-51-5SDS of cas: 2216-51-5).

(1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol (cas: 2216-51-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.SDS of cas: 2216-51-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Habib, Luke et al. published their research in Environmental Science: Atmospheres in 2022 | CAS: 149-32-6

(2R,3S)-rel-Butane-1,2,3,4-tetraol (cas: 149-32-6) 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.Recommanded Product: 149-32-6

Single particle measurements of mixing between mimics for biomass burning and aged secondary organic aerosols was written by Habib, Luke;Donahue, Neil. And the article was included in Environmental Science: Atmospheres in 2022.Recommanded Product: 149-32-6 This article mentions the following:

Gas-phase exchange between aerosol populations via evaporation and condensation of semi-volatile organics can be a major mechanism of mixing between accumulation-mode particles with slow coagulation. This exchange may be impeded in highly viscous, semi-solid, or glassy particles due to diffusion limitations. Here we describe experiments on carefully prepared particle populations representing highly viscous or potentially “glassy” aged organic particles (non-volatile sugars 13C-glucose, sucrose, and raffinose with ammonium sulfate seeds) and fresh biomass burning particles (erythritol with black carbon seeds) to develop a model phase space for organic aerosol systems and better understand when particle phase state impedes mixing. Our hypothesis is that these limitations are alleviated at some relative humidity threshold, which increases with decreasing ambient temperatures We quantify the mixing state of these particle populations from 10-25°C and 5-90% RH using an Aerosol Mass Spectrometer (AMS) combining Event Trigger (ET) and Soot Particle (SP) modes. The observed single particle mass spectra are aggregated in short time slices and used to perform a linear combination of relevant reference spectra to determine the contributions each constituent has on the resulting particle signal. Our results suggest that the non-volatile sugar particles have little to no diffusive limitations to mixing at the conditions tested. In the experiment, the researchers used many compounds, for example, (2R,3S)-rel-Butane-1,2,3,4-tetraol (cas: 149-32-6Recommanded Product: 149-32-6).

(2R,3S)-rel-Butane-1,2,3,4-tetraol (cas: 149-32-6) 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.Recommanded Product: 149-32-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts