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857534-99-7

2-bromo-3-nitro-N-phenylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

857534-99-7

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857534-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857534-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,5,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 857534-99:
(8*8)+(7*5)+(6*7)+(5*5)+(4*3)+(3*4)+(2*9)+(1*9)=217
217 % 10 = 7
So 857534-99-7 is a valid CAS Registry Number.

857534-99-7SDS

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 2-bromo-3-nitro-N-phenylbenzamide

1.2 Other means of identification

Product number -
Other names 2-Brom-3-nitro-benzoesaeure-anilid

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:857534-99-7 SDS

857534-99-7Relevant articles and documents

Nitro-, Azo-, and Amino Derivatives of Ebselen: Synthesis, Structure, and Cytoprotective Effects

Singh, Vijay P.,Poon, Jia-Fei,Yan, Jiajie,Lu, Xi,Ott, Marjam Karlsson,Butcher, Ray J.,Gates, Paul J.,Engman, Lars

, p. 313 - 321 (2017/04/26)

Novel azo-bis-ebselen compounds 7 were prepared by reduction of 7-nitro-2-aryl-1,2-benzisoselenazol-3(2H)-ones 3 and 6 with sodium benzenetellurolate, NaTeC6H5, and by reaction of 2-bromo-3-nitrobenzamides with Na2Se2

Synthesis and glutathione peroxidase-like activities of isoselenazolines

Singh, Vijay P.,Singh, Harkesh B.,Butcher, Ray J.

experimental part, p. 5485 - 5497 (2011/11/29)

The aromatic nucleophilic substitution (SNAr) reactions of N-(2-bromo-3-nitrobenzyl)aniline (18), N-(2-bromo-3-nitrobenzyl)-4-methylaniline (19) and N-(2-bromo-3-nitrobenzyl)-4-nitroaniline (20) with [nBuSeNa] afford N-[2-(butylselanyl)-3-nitro

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