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S-phenyl but-2-enethioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25542-72-7

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25542-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25542-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,4 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25542-72:
(7*2)+(6*5)+(5*5)+(4*4)+(3*2)+(2*7)+(1*2)=107
107 % 10 = 7
So 25542-72-7 is a valid CAS Registry Number.

25542-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name S-phenyl (E)-but-2-enethioate

1.2 Other means of identification

Product number -
Other names Thiocrotonsaeure-S-phenylester

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:25542-72-7 SDS

25542-72-7Relevant academic research and scientific papers

The direct thioesterification of aldehydes with disulfides via NHC-catalyzed carbonyl umpolung strategy

Singh, Santosh,Yadav, Lal Dhar S.

experimental part, p. 5136 - 5140 (2012/09/22)

An efficient N-heterocyclic carbene (NHC)-catalyzed direct thioesterification of aldehydes and α,β-unsaturated aldehydes (enals) with diaryl disulfides is reported. The protocol involves carbonyl umpolung reactivity of aldehydes and enals in which the car

A SIMPLE SYNTHESIS OF THIOL ESTERS FROM COPPER-I-MERCAPTIDES AND ACYL CHLORIDES

Reissig, Hans-Ulrich,Scherer, Bernadette

, p. 4259 - 4262 (2007/10/02)

Thiol esters are obtained from acyl chlorides and copper-I-mercaptides in excellent yields.

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