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41959-35-7

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41959-35-7 Usage

General Description

6-NITRO-1,2,3,4-TETRAHYDRO QUINOXALINE is a chemical compound with the molecular formula C8H8N2O2. It is a nitro-substituted quinoxaline derivative, and is used in the synthesis of pharmaceuticals and other organic compounds. This chemical is known to have neuroprotective and anti-inflammatory properties, and has been studied for its potential use in the treatment of neurodegenerative diseases and inflammatory conditions. It is important to handle this chemical with care, as it may be toxic and harmful if ingested or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 41959-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,5 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41959-35:
(7*4)+(6*1)+(5*9)+(4*5)+(3*9)+(2*3)+(1*5)=137
137 % 10 = 7
So 41959-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O2/c12-11(13)6-1-2-7-8(5-6)10-4-3-9-7/h1-2,5,9-10H,3-4H2

41959-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-1,2,3,4-tetrahydroquinoxaline

1.2 Other means of identification

Product number -
Other names 6-Nitro-1,2,3,4-tetrahydro-chinoxalin

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:41959-35-7 SDS

41959-35-7Downstream Products

41959-35-7Relevant articles and documents

Tetrabutylammonium Bromide-Catalyzed Transfer Hydrogenation of Quinoxaline with HBpin as a Hydrogen Source

Guo, Qi,Chen, Jingchao,Shen, Guoli,Lu, Guangfu,Yang, Xuemei,Tang, Yan,Zhu, Yuanbin,Wu, Shiyuan,Fan, Baomin

, p. 540 - 546 (2021/12/27)

A metal-free environmentally benign, simple, and efficient transfer hydrogenation process of quinoxaline has been developed using the HBpin reagent as a hydrogen source. This reaction is compatible with a variety of quinoxalines offering the desired tetrahydroquinoxalines in moderate-to-excellent yields with Bu4NBr as a noncorrosive and low-cost catalyst.

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