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52736-71-7

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52736-71-7 Usage

General Description

2,3-DIMETHYL-6,7-DICHLOROQUINOXALINE is a chemical compound with the molecular formula C10H6Cl2N2. It is a quinoxaline derivative with two methyl groups and two chlorine atoms attached to the quinoxaline ring. 2,3-DIMETHYL-6,7-DICHLOROQUINOXALINE is used mainly in the pharmaceutical industry as a building block in the synthesis of various pharmaceuticals. It has also been studied for potential applications in the field of organic electronic materials due to its unique molecular structure. Additionally, 2,3-DIMETHYL-6,7-DICHLOROQUINOXALINE has been investigated for its potential biological activities, including anti-cancer and anti-inflammatory properties. Overall, this chemical compound has potential applications in various fields including pharmaceuticals, organic electronics, and biomedical research.

Check Digit Verification of cas no

The CAS Registry Mumber 52736-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,3 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52736-71:
(7*5)+(6*2)+(5*7)+(4*3)+(3*6)+(2*7)+(1*1)=127
127 % 10 = 7
So 52736-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8Cl2N2/c1-5-6(2)14-10-4-8(12)7(11)3-9(10)13-5/h3-4H,1-2H3

52736-71-7SDS

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 6,7-dichloro-2,3-dimethylquinoxaline

1.2 Other means of identification

Product number -
Other names DCDMQ

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:52736-71-7 SDS

52736-71-7Downstream Products

52736-71-7Relevant articles and documents

NaOH-Mediated Direct Synthesis of Quinoxalines from o-Nitroanilines and Alcohols via a Hydrogen-Transfer Strategy

Wang, Yan-Bing,Shi, Linlin,Zhang, Xiaojie,Fu, Lian-Rong,Hu, Weinan,Zhang, Wenjing,Zhu, Xinju,Hao, Xin-Qi,Song, Mao-Ping

, p. 947 - 958 (2021/01/14)

A NaOH-mediated sustainable synthesis of functionalized quinoxalines is disclosed via redox condensation of o-nitroamines with diols and α-hydroxy ketones. Under optimized conditions, various o-nitroamines and alcohols are well tolerated to generate the desired products in 44-99% yields without transition metals and external redox additives.

Quinoxalino-fused sultines and their application in Diels-Alder reactions

Chung, Wen-Sheng,Liu, Jing-Horng

, p. 205 - 206 (2007/10/03)

The synthesis of 7,8-disubstituted quinoxalino[2,3-d]-[1,2λ4]oxathiine 2-oxides 7a-c, precursors for quinoxalino-o-quinodimethanes 3a-c, and their application in the Diels-Alder reactions are reported.

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