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Benzene, 1-[(4-chlorophenyl)sulfonyl]-3-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83627-59-2

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83627-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83627-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,2 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83627-59:
(7*8)+(6*3)+(5*6)+(4*2)+(3*7)+(2*5)+(1*9)=152
152 % 10 = 2
So 83627-59-2 is a valid CAS Registry Number.

83627-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenylsulfonyl)-1-nitrobenzene

1.2 Other means of identification

Product number -
Other names 4'-Chlor-3-nitro-diphenylsulfon

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:83627-59-2 SDS

83627-59-2Relevant academic research and scientific papers

Synthetic study of substituted arylsulfonylphenylbenzamides

Gong, Denghuang,Li, Jiafeng,Yuan, Chengye,Yuan, Junying

, p. 55 - 66 (2007/10/03)

For the structure-activity relationship, a series of substituted arylsulfonyl-phenylbenzamides is reported.

Process for the production of nitro derivatives of aromatic compounds

-

, (2008/06/13)

Nitroderivates of aromatic compounds which are difficult to nitrate, can readily be obtained by nitration providing that the aromatic compound is treated with nitric acid or another nitrating agent in the presence of aliphatic or cycloaliphatic hydrocarbons monosubstituted or polysubstituted by halogen, the nitro group or an alkyl sulphonyl group, and the nitro derivative formed subsequently isolated.

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