Saraswathi Pravallika, M. et al. published their research in European Journal of Biomedical and Pharmaceutical Sciences in 2021 | CAS: 5743-47-5

Calcium 2-hydroxypropanoate pentahydrate (cas: 5743-47-5) 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. 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.Recommanded Product: Calcium 2-hydroxypropanoate pentahydrate

A study on prescription pattern of chronic kidney disease in tertiary care hospital was written by Saraswathi Pravallika, M.;Sampreethi, H.;Anusha, C. H.;Rohini, K.;Shete, Shivkumar. And the article was included in European Journal of Biomedical and Pharmaceutical Sciences in 2021.Recommanded Product: Calcium 2-hydroxypropanoate pentahydrate This article mentions the following:

The aim of the present investigation is to study the prescription pattern of chronic kidney disease in tertiary care hospital. The objective of the study was to study the prescription patterns of drugs used in chronic kidney disease and other comorbid conditions and to identify which drug is mostly prescribed at that hospital. To assess the rationality of prescription. To evaluate the medication adherence in CKD patients. The study on prescribing pattern definitely improves the quality of prescription writing, so study of drug prescribing pattern is relevant in the present scenario. To evaluate the prevalence of correct dosing in chronic kidney diseases depending on renal function estimation This is a retrospective, prospective observational study conducted over a period of six months. The study was conducted at Medicine ward of GLENEAGLES AWARE GLOBAL HOSPITAL LB.NAGAR. Patients who admitted to Nephrol. department of the hospital during a six- month period from Oct. 2021 to March 2021 are enrolled. CKD patients visiting the nephrologists are evaluated, diagnosed and prescribed with suitable therapy. All necessary details were collected from patient demographics, prescription chart, lab data, progress chart, medical records, doctor’s notes, nursing notes using a suitable designed data collection form. One hundred one patients were included in the project; with a mean age of 62.5. ± 18 years. More than half of patients were male, 77(76.2%). The mean BMI was 26 ± 1.15 kg/ m2. The majority of patients were having normal weight 80 (79.2%), 15 (14.8%) patients had overweight, and obesity and only 6 (5.9%) patients were underweight. While 35 (34.6%) patients were smokers, 10 (9.9%) were ex-smokers and 56 (55.4%) patients were non- smokers. Anti- hypertensive agents are predominantly used among the patients. The most preferred options were beta blockers, calcium channel blockers and diuretics. Most of the physicians prescribed metoprolol (18.2%), amlodipine (38.3%), and cilnidipine (2%). Diuretics were the preferred option by the physician furosemide (92.3%), anti-platelets that are prescribed by the physicians are Aspirin (69.2%), clopidogrel (30.7%). Among the lipid lowering agents, atorvastatin (92.8%) was given to the most of the patients. sulbactam (20.4%), cefoperazone (20.4%), clarithromycin (10.25%), amoxycillin (10.25%) were mostly prescribed antibiotics in the study. The study concluded that most of the patients included in the study were suffering from chronic kidney disease. These may be due to their food habits, smoking, less exercise and poor health hygiene. The maximum number of patients was male; it may be due to smoking and alc. habits. Comorbidities such as hypertension, hyperglycemia, albuminuria, renal structure, and sex hormones, have been reported to have different effects on males and females. Thus, CKD progression may differ depending on sex. Early recognition with timely initiation of treatment in collaboration with nephrologists will improve the care for CKD patients. Thus, physicians and Nephrologists play an important outcome in patients with CKD. In the experiment, the researchers used many compounds, for example, Calcium 2-hydroxypropanoate pentahydrate (cas: 5743-47-5Recommanded Product: Calcium 2-hydroxypropanoate pentahydrate).

Calcium 2-hydroxypropanoate pentahydrate (cas: 5743-47-5) 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. 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.Recommanded Product: Calcium 2-hydroxypropanoate pentahydrate

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Schafer, Adam et al. published their research in PLoS Pathogens in 2021 | CAS: 128607-22-7

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Synthetic Route of C24H23ClO2

Evidence for distinct mechanisms of small molecule inhibitors of filovirus entry was written by Schafer, Adam;Xiong, Rui;Cooper, Laura;Nowar, Raghad;Lee, Hyun;Li, Yangfeng;Ramirez, Benjamin E.;Peet, Norton P.;Caffrey, Michael;Thatcher, Gregory R. J.;Saphire, Erica Ollmann;Cheng, Han;Rong, Lijun. And the article was included in PLoS Pathogens in 2021.Synthetic Route of C24H23ClO2 This article mentions the following:

Many small mols. have been identified as entry inhibitors of filoviruses. However, a lack of understanding of the mechanism of action for these mols. limits further their development as anti-filoviral agents. Here we provide evidence that toremifene and other small mol. entry inhibitors have at least three distinctive mechanisms of action and lay the groundwork for future development of anti-filoviral agents. The three mechanisms identified here include: (1) direct binding to the internal fusion loop region of Ebola virus glycoprotein (GP); (2) the HR2 domain is likely the main binding site for Marburg virus GP inhibitors and a secondary binding site for some EBOV GP inhibitors; (3) lysosome trapping of GP inhibitors increases drug exposure in the lysosome and further improves the viral inhibition. Importantly, small mols. targeting different domains on GP are synergistic in inhibiting EBOV entry suggesting these two mechanisms of action are distinct. Our findings provide important mechanistic insights into filovirus entry and rational drug design for future antiviral development. In the experiment, the researchers used many compounds, for example, (Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7Synthetic Route of C24H23ClO2).

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Synthetic Route of C24H23ClO2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Belov, Dmitry S. et al. published their research in Tetrahedron in 2011 | CAS: 40571-86-6

Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6) 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.Safety of Trans-2-(benzylamino)cyclohexanol

Synthesis of (3RS,3aSR,8aSR)-3-phenyloctahydrocyclohepta[b]pyrrol-4(1H)-one via the aza-Cope-Mannich rearrangement was written by Belov, Dmitry S.;Lukyanenko, Evgeny R.;Kurkin, Alexander V.;Yurovskaya, Marina A.. And the article was included in Tetrahedron in 2011.Safety of Trans-2-(benzylamino)cyclohexanol This article mentions the following:

A convenient and scalable method for the preparation of (3RS,3aSR,8aSR)-phenyloctahydrocyclohepta[b]pyrrol-4(1H)-one based on the aza-Cope-Mannich rearrangement is described. This approach allows us to synthesize the target compound in nine steps in a high overall yield (42%) with complete stereocontrol and up to 100 g scale. In the experiment, the researchers used many compounds, for example, Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6Safety of Trans-2-(benzylamino)cyclohexanol).

Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6) 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.Safety of Trans-2-(benzylamino)cyclohexanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kamio, Shintaro et al. published their research in Chemical Communications (Cambridge, United Kingdom) in 2018 | CAS: 68716-49-4

2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 68716-49-4) 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.Reference of 68716-49-4

Anthranilamide (aam)-substituted diboron: palladium-catalyzed selective B(aam) transfer was written by Kamio, Shintaro;Kageyuki, Ikuo;Osaka, Itaru;Hatano, Sayaka;Abe, Manabu;Yoshida, Hiroto. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2018.Reference of 68716-49-4 This article mentions the following:

An unsym. diboron bearing an anthranilamide (aam) substituent was synthesized and was found to be coupled with aryl halides through the palladium-catalyzed Miyaura-Ishiyama-type reaction. The selective transfer of aam-substituted boryl moiety led to exclusive formation of diverse Ar-B(aam). In the experiment, the researchers used many compounds, for example, 2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 68716-49-4Reference of 68716-49-4).

2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (cas: 68716-49-4) 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.Reference of 68716-49-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Chatterjee, Rupak et al. published their research in Asian Journal of Organic Chemistry in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) 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. 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.Product Details of 57-55-6

Bifunctional Metal-free Heterogeneous Catalyst for the Synthesis of Methanol and Diols from CO2 and Epoxide was written by Chatterjee, Rupak;Bhattacharjee, Sudip;Bhaumik, Asim. And the article was included in Asian Journal of Organic Chemistry in 2022.Product Details of 57-55-6 This article mentions the following:

Currently world is facing a serious environmental concern in the steady increase in the CO2 concentration in air and this is directly related to climate change. Thus, successful utilization of CO2 into valuable chems. is one of our primary goals. Herein, we have successfully fabricated a porous organic polymer PDVTA-1 via the free radical cross coupling between divinylbenzene and triallyl amine. This porous polymer is found to possess permanent porosity with a very high BET surface area of 915 m2 g-1. Furthermore, upon sulfonation PDVTA-1 is found to be very active as a bifunctional catalyst with a high BET surface area of 477 m2g-1 and it efficiently catalyzes the synthesis of methanol and diols from CO2 and resp. epoxide under solvent-free process and relatively milder reaction conditions. In this method 34% yield of methanol and 53% propylene glycol are produced from CO2 and propylene oxide by using considerably mild reducing agent Et3SiH. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Product Details of 57-55-6).

1,2-Propanediol (cas: 57-55-6) 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. 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.Product Details of 57-55-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kim, Hyo-Suk et al. published their research in Dalton Transactions in 2015 | CAS: 14123-48-9

1-(Dimethylamino)-2-methylpropan-2-ol (cas: 14123-48-9) 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. 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: 14123-48-9

New heteroleptic magnesium complexes for MgO thin film application was written by Kim, Hyo-Suk;George, Sheby Mary;Park, Bo Keun;Son, Seung Uk;Kim, Chang Gyoun;Chung, Taek-Mo. And the article was included in Dalton Transactions in 2015.Recommanded Product: 14123-48-9 This article mentions the following:

Novel heteroleptic magnesium complexes, [Mg(dmamp)(acac)]2 (1), [Mg(dmamp)(tmhd)]2 (2), [Mg(dmamp)(tfac)]2 (3), and [Mg(dmamp)(hfac)]2 (4), were successfully synthesized using dimethylhydroxyisobutylamine (dmamp) and β-diketonate as ligands. The thermogravimetric analyses and volatile studies of the complexes showed that the complexes 2 and 4 display high volatility and thermal stability. The single crystal x-ray study of the complexes reveals that both the complexes 1 and 2 were crystallized in the triclinic space group and as dimers, where magnesium atoms are in the pentacoordinate state with distorted trigonal bipyramidal geometry. In the experiment, the researchers used many compounds, for example, 1-(Dimethylamino)-2-methylpropan-2-ol (cas: 14123-48-9Recommanded Product: 14123-48-9).

1-(Dimethylamino)-2-methylpropan-2-ol (cas: 14123-48-9) 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. 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: 14123-48-9

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zhang, Mei et al. published their research in Materials Letters in 2022 | CAS: 111-46-6

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 111-46-6

Efficient oxygen evolution photocatalyst of BiOBr: In situ light-induced formation of surface oxygen vacancies and application in water splitting was written by Zhang, Mei;Xie, Fangxia;Zhang, Lulu;Jian, Xuan;Liu, Jianxin;Zhang, Xiaochao;Wang, Yawen;Li, Rui;Fan, Caimei. And the article was included in Materials Letters in 2022.SDS of cas: 111-46-6 This article mentions the following:

The slow rate of oxygen evolution severely limits the overall water splitting, constructing oxygen vacancies on the surface of photocatalysts is an effective strategy in improving the performance of catalysts. However, the oxygen vacancies can be easily renovated by the adsorbed water and oxygen, then deactivating the catalysts. Herein, we synthesized a nanoflower BiOBr, which could produce continuously sufficient OVs induced by light during the photocatalytic water splitting, and investigated the effect of OVs concentration on the performance of photocatalytic O2 evolution. The results showed that the sustainable light-induced OVs could improve the transfer efficiency of photoinduced carriers and the light absorption capacity, which then cause a significant increase in reaction rates. The optimal oxygen evolution rate could reach 166μmol·g-1·h-1. This work provides a new way of constructing sustainable oxygen vacancies on the surface of catalysts toward photocatalytic water splitting. In the experiment, the researchers used many compounds, for example, 2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6SDS of cas: 111-46-6).

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 111-46-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Pinto, Tania V. et al. published their research in ACS Agricultural Science & Technology in 2022 | CAS: 499-75-2

5-Isopropyl-2-methylphenol (cas: 499-75-2) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 499-75-2

Micro- and Nanocarriers for Encapsulation of Biological Plant Protection Agents: A Systematic Literature Review was written by Pinto, Tania V.;Silva, Claudia A.;Siquenique, Sonia;Learmonth, David A.. And the article was included in ACS Agricultural Science & Technology in 2022.HPLC of Formula: 499-75-2 This article mentions the following:

Biol. plant protection agents (BPPAs) are proposed as sustainable alternatives to chem.-based pesticides to face threats caused by pests and diseases emerging due to climate change. The present Review was conducted to identify the most promising materials to encapsulate and deliver BPPAs for pest and disease control with improved efficacy, increased systemic activity, and lower environmental impact. Searches on Scopus and Web of Science databases from inception up to June 30, 2022, revealed a total of 98 reports that met the eligibility criteria, 45% of which described the use of (1) naturally sourced polymers, such as chitosan (36%), alginate (23%) and plant-based proteins (16%); (2) synthetic polymers (35%); (3) inorganic materials (19%); and (4) microorganisms (1%). The review confirmed that micro- and nanoencapsulation of BPPAs using carrier materials of marine/terrestrial/synthetic sources should provide the agricultural community access to safer and more sustainable plant protection products. In the experiment, the researchers used many compounds, for example, 5-Isopropyl-2-methylphenol (cas: 499-75-2HPLC of Formula: 499-75-2).

5-Isopropyl-2-methylphenol (cas: 499-75-2) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 499-75-2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Shen, Dong-Yu et al. published their research in Journal of Food Composition and Analysis in 2023 | CAS: 3391-86-4

Oct-1-en-3-ol (cas: 3391-86-4) 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. 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.Recommanded Product: 3391-86-4

Characterization of key odor-active compounds in pure chicken powder and the effect of yeast extract, using instrumental and sensory techniques was written by Shen, Dong-Yu;Li, Meng-Ke;Zhao, Mu;Li, Jie;Cui, Xinyue;Zou, Ting-Ting;Song, Huan-Lu;Xiong, Jian;Li, Ku. And the article was included in Journal of Food Composition and Analysis in 2023.Recommanded Product: 3391-86-4 This article mentions the following:

Pure chicken powder (PCP) is a reliable source of mellow chicken soup flavor in seasoning, but it has some unstable compounds and is prone to lipid oxidation, which leads to unpleasant odor. Adding yeast extract (YE) can reduce the off-odor intensity of PCP. Based on the results of gas chromatog.-olfactometry-mass spectrometry (GC-O-MS), two-dimensional comprehensive gas chromatog.-olfactometry-mass spectrometry (GCxGC-O-MS) and combined aroma extract dilution anal. (AEDA), 14 key odor-active compounds were identified. Internal standard curve method was used for quant. anal., and the odor activity value (OAV) was calculated Octanal, 1-octen-3-ol and hexanal were found to be the most vital odor-active compounds in PCP. The odor-active compounds of YE were studied by the same method, and di-Me trisulfide was identified as the most important odor-active compound of YE. Addnl., recombination and omission experiments were carried out with PCP. Finally, it was found that a low concentration of di-Me trisulfide had masking effect on the odor of PCP. In the experiment, the researchers used many compounds, for example, Oct-1-en-3-ol (cas: 3391-86-4Recommanded Product: 3391-86-4).

Oct-1-en-3-ol (cas: 3391-86-4) 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. 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.Recommanded Product: 3391-86-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Comely, Alex C. et al. published their research in Journal of the American Chemical Society in 2003 | CAS: 60463-12-9

3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9) 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.Quality Control of 3-(Hydroxymethyl)-4-nitrophenol

De Novo Asymmetric Bio- and Chemo-Catalytic Synthesis of Saccharides – Stereoselective Formal O-Glycoside Bond Formation Using Palladium Catalysis was written by Comely, Alex C.;Eelkema, Rienk;Minnaard, Adriaan J.;Feringa, Ben L.. And the article was included in Journal of the American Chemical Society in 2003.Quality Control of 3-(Hydroxymethyl)-4-nitrophenol This article mentions the following:

A novel integrated bio- and chemo-catalytic approach to the de novo catalytic asym. synthesis of saccharides has been developed. Acetoxypyranones obtained enantiopure by enzymic resolution have been shown to undergo highly stereoselective palladium-catalyzed formal O-glycoside bond formation. The combination of these protocols can be applied to asym. catalytic synthesis of saccharides. In the experiment, the researchers used many compounds, for example, 3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9Quality Control of 3-(Hydroxymethyl)-4-nitrophenol).

3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9) 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.Quality Control of 3-(Hydroxymethyl)-4-nitrophenol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts