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934-78-1

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934-78-1 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.

Check Digit Verification of cas no

The CAS Registry Mumber 934-78-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 934-78:
(5*9)+(4*3)+(3*4)+(2*7)+(1*8)=91
91 % 10 = 1
So 934-78-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-6-4-3-5-8(9-6)7(2)10/h3-5,7,10H,1-2H3

934-78-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-methylpyridin-2-yl)ethanol

1.2 Other means of identification

Product number -
Other names EINECS 213-292-1

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:934-78-1 SDS

934-78-1Relevant articles and documents

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

Seath, Ciaran P.,Vogt, David B.,Xu, Zihao,Boyington, Allyson J.,Jui, Nathan T.

supporting information, p. 15525 - 15534 (2018/11/23)

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

Murakoshi,Kubo,Saito,Haginiwa

, p. 900 - 902 (2007/10/04)

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