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2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62292-40-4

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62292-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62292-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,9 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62292-40:
(7*6)+(6*2)+(5*2)+(4*9)+(3*2)+(2*4)+(1*0)=114
114 % 10 = 4
So 62292-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H11ClN2O3S/c15-9-14(18)16-10-1-5-12(6-2-10)21-13-7-3-11(4-8-13)17(19)20/h1-8H,9H2,(H,16,18)

62292-40-4SDS

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-Chloro-N-{4-[(4-nitrophenyl)-thio]phenyl}acetamide

1.2 Other means of identification

Product number -
Other names 2-Chloro-N-[4-[(4-nitrophenyl)thio]phenyl]acetamide

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:62292-40-4 SDS

62292-40-4Relevant academic research and scientific papers

2-Amino-4'(phenylsulfonyl) acetanilides

-

, (2008/06/13)

A method of modulating the immune response system in a warm-blooded animal by the administration of N-substituted-phenylthioanilines, N-substituted-phenylsulfinylanilines, and N-substituted-phenylsulfonylanilines, certain of which are new compounds.

Synthesis and Biological Activity of Some New Diaryl Sulphides and Diaryl Sulphones Containing Amino Acid Moieties

Abbady, M. A.,Ali, M. M.,Kandeel, M. M.

, p. 53 - 57 (2007/10/02)

N-Phthaloylaminoacid chlorides (IIa-c) react with 4-amino-4'-nitrodiphenyl sulphide (Ia) and 4-amino-2'-nitrodiphenyl sulphide (Ib) in dioxane in the presence of triethylamine to give N-(N'-phthaloylaminoacyl)-4-aminodiphenyl sulphides (IIIa-b), the hydra

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