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61174-18-3

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61174-18-3 Usage

Type of compound

Nitrobenzene derivative

Structure

Contains a benzene ring with a nitro group (-NO2) and a sulfonyl group (-SO2) attached to it

Appearance

Yellow crystalline powder

Uses

a. Synthesis of pharmaceuticals and agrochemicals
b. Reagent in organic chemistry reactions
c. Synthesis of various organic compounds

Sulfonyl group property

Strong electron-withdrawing properties

Utility

Useful intermediate in organic synthesis

Safety precautions

Handle with care due to potential hazards to health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 61174-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,7 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61174-18:
(7*6)+(6*1)+(5*1)+(4*7)+(3*4)+(2*1)+(1*8)=103
103 % 10 = 3
So 61174-18-3 is a valid CAS Registry Number.

61174-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)sulfonyl-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 4'-Chlor-2-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:61174-18-3 SDS

61174-18-3Relevant articles and documents

Silver-promoted decarboxylative sulfonylation of aromatic carboxylic acids with sodium sulfinates

Yu, Yongqi,Wu, Qianlong,Liu, Da,Yu, Lin,Tan, Ze,Zhu, Gangguo

, p. 11195 - 11202 (2019/09/12)

A novel and efficient synthesis of sulfones was developed via a silver-promoted decarboxylative sulfonylation reaction between aromatic carboxylic acids and sodium sulfinates for the first time. The approach features operational simplicity and good functional group compatibility and uses readily available starting materials. Furthermore, mechanistic studies reveal that the decarboxylative sulfonylation reaction is likely to proceed via a radical mechanism.

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