CAS 102074-19-1

(5-METHYLPYRIDIN-3-YL)METHANOL

Description:

(5-Methylpyridin-3-yl)methanol, with the CAS number 102074-19-1, is an organic compound characterized by the presence of a pyridine ring substituted with a methyl group and a hydroxymethyl group. This compound features a five-membered aromatic ring containing nitrogen, which contributes to its basicity and potential reactivity. The hydroxymethyl group (-CH2OH) enhances its solubility in polar solvents and may participate in hydrogen bonding, influencing its physical properties and reactivity. The presence of the methyl group at the 5-position of the pyridine ring can affect the electronic distribution and steric hindrance, impacting its interactions with other molecules. This compound may be of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential biological activity and utility as a building block in organic synthesis. Its stability, reactivity, and specific applications would depend on the conditions under which it is used, including temperature, pH, and the presence of other reagents.

Formula: C₇H₉NO

InChI: InChI=1/C7H9NO/c1-6-2-7(5-9)4-8-3-6/h2-4,9H,5H2,1H3

SMILES: Cc1cc(cnc1)CO

Synonyms:

• 3-Pyridinemethanol, 5-methyl-
• 5-Methyl-3-pyridinemethanol

3-Pyridinemethanol, 5-methyl-

CAS: 102074-19-1

Formula: C₇H₉NO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 123.1525

Ref: IN-DA0006L6

(5-Methylpyridin-3-yl)methanol

CAS: 102074-19-1

(5-Methylpyridin-3-yl)methanol

Formula: C₇H₉NO

Purity: 95%

Color and Shape: light brown liquid

Molecular weight: 123.15g/mol

Ref: 54-OR932347

Nicotine Related Compound 3

CAS: 102074-19-1

Formula: C₇H₉NO

Molecular weight: 123.16

Ref: 4Z-N-0692

(5-Methylpyridin-3-yl)methanol

CAS: 102074-19-1

Formula: C₇H₉NO

Purity: 97%

Color and Shape: Liquid

Molecular weight: 123.155

Ref: 10-F325071

5-Methyl-3-pyridinemethanol

CAS: 102074-19-1

5-Methyl-3-pyridinemethanol is an organic compound that is used in the preparation of rupatadine, a drug used to treat allergic rhinitis. It is prepared by reduction of 5-methyl-3-pyridinecarboxaldehyde with sodium borohydride in an organic solvent at room temperature. The reaction system must be free of oxygen and moisture and the reaction conditions are carried out under high yield and at large scales. The product is purified by crystallization from chloroform or hydrobromide in order to remove impurities.

Formula: C₇H₉NO

Purity: Min. 95%

Molecular weight: 123.15 g/mol

Ref: 3D-CEA07419