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141884-92-6

4-bromomethyl-3-nitrobenzoic acid succinimide ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141884-92-6

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141884-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141884-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,8,8 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141884-92:
(8*1)+(7*4)+(6*1)+(5*8)+(4*8)+(3*4)+(2*9)+(1*2)=146
146 % 10 = 6
So 141884-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H6BrNO4.C4H5NO2/c9-4-6-2-1-5(8(11)12)3-7(6)10(13)14;6-3-1-2-4(7)5-3/h1-3H,4H2,(H,11,12);1-2H2,(H,5,6,7)

141884-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(bromomethyl)-3-nitrobenzoic acid,pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 4-Bromomethyl-3-nitrobenzoic acid succinimide ester

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:141884-92-6 SDS

141884-92-6Relevant articles and documents

Synthesis and evaluation of the anti parasitic activity of aromatic nitro compounds

Lopes, Marcela S.,De Souza Pietra, Renata C.C.,Borgati, Tatiane F.,Romeiro, Carla F.D.,Júnior, Policarpo A.S.,Romanha, Alvaro J.,Alves, Ricardo J.,Souza-Fagundes, Elaine M.,Fernandes, Ana Paula S.M.,De Oliveira, Renata B.

, p. 5443 - 5447 (2011/12/15)

A series of nitroaromatic compounds was synthesized and evaluated as potential antileishmanial and trypanocidal agents. Five compounds exerted significant anti-leishmanial activity in vitro against promastigotes forms of Leishmania (L.) amazonensis, with

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