934-78-1

Basic information

• Product Name: 2-(HYDROXYETHYL)-6-METHYLPYRIDINE
• Synonyms: 2-(HYDROXYETHYL)-6-METHYLPYRIDINE;6-METHYL-2-PYRIDINE ETHANOL;6-methylpyridine-2-ethanol;2-(6-Methyl-2-pyridyl)ethanol;PYRIDINEETHANOL,6-METHYL-
• CAS NO: 934-78-1
• Molecular Formula: C₈H₁₁NO
• Molecular Weight: 137.18
• EINECS: 213-292-1
• Mol File: 934-78-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 56 °C
• Boiling Point: 226.3 °C at 760 mmHg
• Flash Point: 90.6 °C
• Appearance: /
• Density: 1.061 g/cm³
• Vapor Pressure: 0.0759mmHg at 25°C
• Refractive Index: 1.531
• PKA: 14.73±0.10(Predicted)
• CAS DataBase Reference: 2-(HYDROXYETHYL)-6-METHYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(HYDROXYETHYL)-6-METHYLPYRIDINE(934-78-1)
• EPA Substance Registry System: 2-(HYDROXYETHYL)-6-METHYLPYRIDINE(934-78-1)

Safety Data

• Hazardous Substances Data: 934-78-1(Hazardous Substances Data)

Usage

General Description

2-(Hydroxyethyl)-6-methylpyridine is a chemical compound with the formula C8H11NO. It is a derivative of pyridine with a hydroxyethyl group at the 2-position and a methyl group at the 6-position. 2-(HYDROXYETHYL)-6-METHYLPYRIDINE is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a reagent in organic synthesis and as a building block for the production of various commercial products. Additionally, it has some biological activity and has been studied for its potential use in medicinal applications.

InChI:InChI=1/C8H11NO/c1-6-4-3-5-8(9-6)7(2)10/h3-5,7,10H,1-2H3

Upstream product

• 108-48-5 2,6-dimethylpyridine 
• 50-00-0 formaldehyd 
• 1611489-44-1 2-methyl-6-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)pyridine 
• 7732-18-5 water 

Downstream Products

• 1450633-79-0 2-methyl-6-(2-phenoxyethyl)piperidine 
• 1450633-78-9 2-methyl-6-(2-phenoxyethyl)pyridine 
• 1411980-58-9 2-(2-(6-methylpyridin-2-yl)ethyl)-7-(4-(trifluoromethoxy)phenyl)phthalazin-1(2H)-one 
• 1104382-68-4 1-methyl-6-{4-[2-(6-methyl-pyridin-2-yl)-ethoxy]-3-(trifluoromethyl)-phenyl}-1H-imidazo[4,5-c]pyridine-4-carbonitrile trifluoroacetate 
• 1196-40-3 cis-4-methylquinolizidine 
• 1196-40-3 trans-4-methylquinolizidine 
• 856857-19-7 (6-ethyl-[2]pyridyl)-acetic acid ethyl ester 
• 1122-69-6 2-ethyl-6-methylpyridine 
• 136401-73-5 5-<4-<2-(6-Methyl-2-pyridyl)ethoxy>benzylidene>rhodanine-3-acetic Acid 
• 136401-76-8 5-<4-<2-(6-Methyl-2-pyridyl)ethoxy>benzylidene>-2-thioxo-5-thiazolidinone 
• 136401-72-4 5-<4-<2-(6-Methyl-2-pyridyl)ethoxy>benzylidene>rhodanine 
• 136401-66-6 5-<4-<2-(6-Methyl-2-pyridyl)ethoxy>benzylidene>-2,4-thiazolidinedione 
• 136401-75-7 5-<4-<2-(6-Methyl-2-pyridyl)ethoxy>benzylidene>-2-thiohydantoin 
• 136401-74-6 5-<4-<2-(6-Methyl-2-pyridyl)ethoxy>benzylidene>hydantoin 

Relevant articles and documents

Radical Hydroarylation of Functionalized Olefins and Mechanistic Investigation of Photocatalytic Pyridyl Radical Reactions

We report the photoredox alkylation of halopyridines using functionalized alkene and alkyne building blocks. Selective single-electron reduction of the halogenated pyridines provides the corresponding heteroaryl radicals, which undergo anti-Markovnikov addition to the alkene substrates. The system is shown to be mild and tolerant of a variety of alkene and alkyne subtypes. A combination of computational and experimental studies support a mechanism involving proton-coupled electron transfer followed by medium-dependent alkene addition and rapid hydrogen atom transfer mediated by a polarity-reversal catalyst.

A new synthetic method of cyclic nitrogenous compounds. XIV. Synthesis of 1,2,3,5,6,6a,7,8,9,9a-decahydropyrido-[2,1,6-de]quinolizine derivatives

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