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Benzenesulfonothioic acid, 4-methyl-, S-2-benzoxazolyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87559-81-7

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87559-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87559-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,5 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87559-81:
(7*8)+(6*7)+(5*5)+(4*5)+(3*9)+(2*8)+(1*1)=187
187 % 10 = 7
So 87559-81-7 is a valid CAS Registry Number.

87559-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoxazolyl-2 toluene thiosulfonate

1.2 Other means of identification

Product number -
Other names benzoxazol-2-yl p-toluenethiosulfonate

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:87559-81-7 SDS

87559-81-7Downstream Products

87559-81-7Relevant academic research and scientific papers

A FACILE SYNTHESIS OF UNSYMMETRICAL THIOSULFONATES VIA SULFONYLATION OF MERCAPTANS

Ranasinghe, M. G.,Fuchs, P. L.

, p. 227 - 232 (2007/10/02)

The reaction of p-toluenesulfonyl bromide with mercaptans provides a convenient procedure for the synthesis of unsymmetrical thiolsulfonates.

SYNTHESIS OF NEW THIOSULFONATES AND DISULFIDES FROM SULFONYL CHLORIDES AND THIOLS

Mahieu, Jean-Pierre,Gosselet, Martine,Sebille, Bernard,Beuzard, Yves

, p. 1709 - 1722 (2007/10/02)

Aromatic thiols were converted into thiosulfonates or disulfides, under very mild conditions, with fair to excellent yields, by using sulfonyl chloride as oxydant reagent.

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