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Benzenemethanesulfonamide, N-(2-amino-4,5-dimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

400889-57-8

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400889-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 400889-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,8,8 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 400889-57:
(8*4)+(7*0)+(6*0)+(5*8)+(4*8)+(3*9)+(2*5)+(1*7)=148
148 % 10 = 8
So 400889-57-8 is a valid CAS Registry Number.

400889-57-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-amino-4,5-dimethylphenyl)-1-phenylmethanesulfonamide

1.2 Other means of identification

Product number -
Other names N-benzylsulfonyl-4,5-dimethyl-o-phenylenediamine

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:400889-57-8 SDS

400889-57-8Downstream Products

400889-57-8Relevant academic research and scientific papers

Tautomerism and stereodynamics of indophenols, amidines, and their derivatives and analogs: XVI. Synthesis of tetrahydroquinoxalines having spiro-fused oxoindole and cyclohepta[c]furan fragments

Kurbatov,Kuznetsov,Simakov,Voronina,Zhdanov,Olekhnovich

, p. 731 - 737 (2004)

Alkylation of o-(N-sulfonylamino)phenylimino derivatives of indol-2-one and cyclohepta[c]furan with phenacyl bromides is accompanied by cyclization to previously unknown tetrahydroquinoxalines having spiro-fused oxoindole and cyclohepta[c]furan fragments. The structure of the latter includes a nitrogen-oxygen triangular system typical of most natural cytotoxic compounds.

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