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

38676-16-3

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38676-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38676-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,7 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38676-16:
(7*3)+(6*8)+(5*6)+(4*7)+(3*6)+(2*1)+(1*6)=153
153 % 10 = 3
So 38676-16-3 is a valid CAS Registry Number.

38676-16-3SDS

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 (toluene-4-sulfonyl)-m-tolyl-diazene

1.2 Other means of identification

Product number -
Other names N'-p-Toluolsulfonyl-N-m-tolyl-diimid

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:38676-16-3 SDS

38676-16-3Downstream Products

38676-16-3Relevant academic research and scientific papers

Modular Synthesis of Alkylarylazo Compounds via Iron(III)-Catalyzed Olefin Hydroamination

Zhang, Yan,Huang, Chenchao,Lin, Xinru,Hu, Qi,Hu, Boyue,Zhou, Yulu,Zhu, Gangguo

, p. 2261 - 2264 (2019/03/26)

A novel Fe-catalyzed olefin hydroamination with aryldiazo sulfones for accessing alkylarylazo compounds has been successfully developed. Aryldiazo sulfones are used as radical acceptors, and N-N double bonds will be regenerated when an arene sulfonyl grou

Copper-catalyzed synthesis of aryldiazo sulfones from arylhydrazines and sulfonyl chlorides under mild conditions

Liu, Jin-Biao,Chen, Fu-Jiao,Liu, En,Li, Jin-Hui,Qiu, Guanyinsheng

supporting information, p. 7773 - 7776 (2015/10/12)

In this paper, aryldiazo sulfones are prepared from tandem sulfonylation/dehydrogenation reactions of arylhydrazines and sulfonyl chlorides. The transformations proceed well in the presence of catalytic CuSO4·5H2O, leading to aryldiazo sulfones in good to excellent yields. It is believed that this protocol represents a safe and convenient model for the synthesis of these versatile aryldiazo sulfones under mild conditions.

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