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4-acetamidophenyl benzyl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92850-44-7

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92850-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92850-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,5 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92850-44:
(7*9)+(6*2)+(5*8)+(4*5)+(3*0)+(2*4)+(1*4)=147
147 % 10 = 7
So 92850-44-7 is a valid CAS Registry Number.

92850-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetamidophenyl benzyl sulfide

1.2 Other means of identification

Product number -
Other names benzyl 4-nitrophenyl sulfide

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:92850-44-7 SDS

92850-44-7Relevant academic research and scientific papers

I2-catalyzed oxidative C(sp3)-H/S-H coupling: Utilizing alkanes and mercaptans as the nucleophiles

Yuan, Jiwen,Ma, Xu,Yi, Hong,Liu, Chao,Lei, Aiwen

supporting information, p. 14386 - 14389 (2014/12/11)

By using alkanes and mercaptans as the nucleophiles with di-tert-butyl peroxide (DTBP) as the oxidant, I2-catalyzed oxidative C(sp3)-H/S-H coupling was achieved. This protocol provides a novel process to construct C(sp3)-S bonds from commercially available hydrocarbons and mercaptans.

A simple and efficient method for preparation of unsymmetrical sulfides

Yin, Jianming,Pidgeon, Charles

, p. 5953 - 5954 (2007/10/03)

A simple and high efficient method for preparation of unsymmetrical sulfides is described.

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