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2427-71-6

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2427-71-6 Usage

Chemical Properties

Crystalline Powder

Uses

Intermediate for the production of herbicides. Attributes PIS available, please contact us Contact

Check Digit Verification of cas no

The CAS Registry Mumber 2427-71-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2427-71:
(6*2)+(5*4)+(4*2)+(3*7)+(2*7)+(1*1)=76
76 % 10 = 6
So 2427-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClN2O/c9-5-1-2-6-7(3-5)10-4-8(12)11-6/h1-4H,(H,11,12)

2427-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-6-chloroquinoxaline

1.2 Other means of identification

Product number -
Other names 6-chloroquinoxalin-2-one

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:2427-71-6 SDS

2427-71-6Relevant articles and documents

Electro-oxidative C-H alkylation of quinoxalin-2(1: H)-ones with organoboron compounds

Niu, Kaikai,Hao, Yanke,Song, Lingyun,Liu, Yuxiu,Wang, Qingmin

supporting information, p. 302 - 306 (2021/01/28)

Radical cleavage of C-B bonds to accomplish C-H functionalization is synthetically appealing but practically challenging. We report herein a mild electro-oxidative method for efficient C-H alkylation of quinoxalin-2(1H)-ones by means of radical addition reactions of alkyl boronic acids and esters and alkyl trifluoroborates to afford C-C coupled products. This journal is

The facile one pot synthesis of 6-substituted 2(1H)-quinoxalinones

Sakata, Gozyo,Makino, Kenzi,Morimoto, Katsushi

, p. 143 - 151 (2007/10/02)

Facile one pot synthesis of 6-substituted 2(1H)-quinoxalinones and these reaction mechanisms are described.The intramolecular cyclization reaction of 4'-substituted 2'-nitroacetoacetanilides in aqueous basic medium and the reduction of 6-substituted 2(1H)-quinoxalinone-4-oxide wit sodium borohydride or sodium hydrogensulfite were studied in detail

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