Category: 102074-19-1

Modyanova, L. V. et al. published their research in Biotekhnologiya in 1990 | CAS: 102074-19-1

(5-Methylpyridin-3-yl)methanol (cas: 102074-19-1) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 102074-19-1

Microbial transformation of nitrogen-containing heterocyclic compounds. I. Hydroxylation of isomeric mono- and dimethylpyridines by microscopic fungi was written by Modyanova, L. V.;Vorob’eva, L. I.;Shibilkina, O. K.;Dovgilevich, E. V.;Terent’ev, P. B.;Kost, A. N.. And the article was included in Biotekhnologiya in 1990.HPLC of Formula: 102074-19-1 This article mentions the following:

By screening a number of museum microorganism cultures a group of microscopic fungi active in transforming mono- and dimethylpyridines was detected. It is only the Me substituent that undergoes oxidation, not the pyridine ring itself. Peculiarities of oxidative transformation of isomeric mono- and dimethylpyridines to the corresponding hydroxymethylpyridines were elucidated. For methylpyridines the pyridylcarbinol yield was independent of the Me substituent position. For dimethylpyridines only 1 Me group is subjected to hydroxylation, the ratio of the pyridylcarbinols obtained mainly depending on the substituent arrangement in the pyridine ring. In the experiment, the researchers used many compounds, for example, (5-Methylpyridin-3-yl)methanol (cas: 102074-19-1HPLC of Formula: 102074-19-1).

(5-Methylpyridin-3-yl)methanol (cas: 102074-19-1) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 102074-19-1

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Chavakula, Ramadas et al. published their research in Journal of the Indian Chemical Society in 2014 | CAS: 102074-19-1

(5-Methylpyridin-3-yl)methanol (cas: 102074-19-1) 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.Application In Synthesis of (5-Methylpyridin-3-yl)methanol

Industrially viable process for reduction of esters to alcohols with sodium borohydride under buffer and aqueous alcoholic conditions was written by Chavakula, Ramadas;Rao, M. Narayana;Babu, B. Gopi;Kumar, K. Praveen;Rao, Ch. Srinivasa. And the article was included in Journal of the Indian Chemical Society in 2014.Application In Synthesis of (5-Methylpyridin-3-yl)methanol This article mentions the following:

A simple and convenient procedure for the synthesis of alcs. from esters by reduction method using sodium borohydride in the presence of dipotassium hydrogen orthophosphate under aqueous alc. conditions is described. This method uses inexpensive, safe and environmentally friendly reducing agent. In the experiment, the researchers used many compounds, for example, (5-Methylpyridin-3-yl)methanol (cas: 102074-19-1Application In Synthesis of (5-Methylpyridin-3-yl)methanol).

(5-Methylpyridin-3-yl)methanol (cas: 102074-19-1) 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.Application In Synthesis of (5-Methylpyridin-3-yl)methanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Chavakula, Ramadas et al. published their research in Journal of the Indian Chemical Society in 2014 | CAS: 102074-19-1

(5-Methylpyridin-3-yl)methanol (cas: 102074-19-1) 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.Application In Synthesis of (5-Methylpyridin-3-yl)methanol

Industrially viable process for reduction of esters to alcohols with sodium borohydride under buffer and aqueous alcoholic conditions was written by Chavakula, Ramadas;Rao, M. Narayana;Babu, B. Gopi;Kumar, K. Praveen;Rao, Ch. Srinivasa. And the article was included in Journal of the Indian Chemical Society in 2014.Application In Synthesis of (5-Methylpyridin-3-yl)methanol This article mentions the following:

A simple and convenient procedure for the synthesis of alcs. from esters by reduction method using sodium borohydride in the presence of dipotassium hydrogen orthophosphate under aqueous alc. conditions is described. This method uses inexpensive, safe and environmentally friendly reducing agent. In the experiment, the researchers used many compounds, for example, (5-Methylpyridin-3-yl)methanol (cas: 102074-19-1Application In Synthesis of (5-Methylpyridin-3-yl)methanol).

(5-Methylpyridin-3-yl)methanol (cas: 102074-19-1) 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.Application In Synthesis of (5-Methylpyridin-3-yl)methanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts