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1-nitro-2-((3-nitrophenyl)sulfonyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34418-84-3

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34418-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34418-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,1 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34418-84:
(7*3)+(6*4)+(5*4)+(4*1)+(3*8)+(2*8)+(1*4)=113
113 % 10 = 3
So 34418-84-3 is a valid CAS Registry Number.

34418-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3'-dinitrodiphenyl sulfone

1.2 Other means of identification

Product number -
Other names (2-Nitro-phenyl)-(3-nitro-phenyl)-sulfon

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:34418-84-3 SDS

34418-84-3Relevant academic research and scientific papers

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.

Convenient one-pot procedure for converting aryl sulfides to nitroaryl sulfones

Nose, Masatoshi,Suzuki, Hitomi

, p. 1065 - 1071 (2007/10/03)

When treated with nitrogen dioxide and ozone in inert solvent at 0°C or below, aryl sulfides underwent smooth oxidative nitration to give nitroaryl sulfones in good yield. Using this methodology, a series of mono- and di-nitrated aryl sulfones were prepared from methyl phenyl sulfide and diphenyl sulfide and their physical data are presented.

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