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Benzenemethanol, 4-(methylthio)-a-(trifluoromethyl)-, 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116703-74-3

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116703-74-3 Usage

Chemical compound

Benzenemethanol, 4-(methylthio)-α-(trifluoromethyl)-, 4-methylbenzenesulfonate

Structure

consists of a benzene ring with a methanol group, a trifluoromethyl group, a methylthio group, and a 4-methylbenzenesulfonate group

Industrial applications

potential uses in pharmaceuticals, agrochemicals, and materials science

Specific properties and uses

would need further research and testing to determine

Check Digit Verification of cas no

The CAS Registry Mumber 116703-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,0 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116703-74:
(8*1)+(7*1)+(6*6)+(5*7)+(4*0)+(3*3)+(2*7)+(1*4)=113
113 % 10 = 3
So 116703-74-3 is a valid CAS Registry Number.

116703-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-(Methylthio)phenyl)-2,2,2-trifluoroethyl tosylate

1.2 Other means of identification

Product number -
Other names Toluene-4-sulfonic acid 2,2,2-trifluoro-1-(4-methylsulfanyl-phenyl)-ethyl ester

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:116703-74-3 SDS

116703-74-3Downstream Products

116703-74-3Relevant academic research and scientific papers

The Extraordinarily Long Lifetimes and Other Properties of Highly Destabilized Ring-Substituted 1-Phenyl-2,2,2-trifluoroethyl Carbocations

Richard, John P.

, p. 1455 - 1465 (2007/10/02)

A large bromide common ion rate depression is observed for the reactions of 1-(4-methoxyphenyl)- and 1-(4-(methylthio)phenyl)-2,2,2-trifluoroethyl bromides in largely aqueous solutions when the ionic strenght is maintained with weakly nucleophilic NaClO4

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