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79623-37-3

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79623-37-3 Usage

General Description

2(3H)-PYRIDINONE, 3-CHLORO-5-(TRIFLUOROMETHYL)- is a chemical compound with the molecular formula C7H4ClF2NO. It is a heterocyclic compound that contains a pyridinone ring with a chlorine atom and a trifluoromethyl group attached to it. 2(3H)-PYRIDINONE, 3-CHLORO-5-(TRIFLUOROMETHYL)- is used in the synthesis of pharmaceuticals and agrochemicals, and it has potential applications in the field of medicinal chemistry. It is important to handle this compound with caution as it may be hazardous if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 79623-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,2 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79623-37:
(7*7)+(6*9)+(5*6)+(4*2)+(3*3)+(2*3)+(1*7)=163
163 % 10 = 3
So 79623-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClF3NO/c7-4-1-3(6(8,9)10)2-11-5(4)12/h1-2,4H

79623-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-5-(trifluoromethyl)-2(1H)-pyridinone

1.2 Other means of identification

Product number -
Other names 3-Chloro-5-(trifluoromethyl)-2(3H)-pyridinone

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:79623-37-3 SDS

79623-37-3Downstream Products

79623-37-3Relevant articles and documents

Alcoholysis of trifluoromethyl groups attached to the pyridine ring

Qian, Xuhong,Liu, Shuyou

, p. 9 - 12 (2007/10/03)

In dimethylformamide solution, trifluoroethoxylation and methoxylation of 5-chloro-3-trifluoromethylpyridine (2) yield 5-chloro-3-tris(trifluoroethoxyl)methyl pyridine (2a) and a dimethyl ketal of 3-chloronicotinic acid anhydride (2b) with fluorines as leaving groups, respectively. The corresponding reactions of 2,3-dichloro-5-trifluoromethylpyridine (3) only yield the 2-alkoxy-substituted products 3a and 3b with chloro as the leaving group and the 2-dimethylamino product 3c which was formed by the action of solvent dimethylformamide as a nucleophile. Differences in their reaction behaviour and possible mechanisms are also discussed.

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