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Benzene, 3-[(4-chlorophenyl)thio]-1,2,4,5-tetramethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77304-54-2

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77304-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77304-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 77304-54:
(7*7)+(6*7)+(5*3)+(4*0)+(3*4)+(2*5)+(1*4)=132
132 % 10 = 2
So 77304-54-2 is a valid CAS Registry Number.

77304-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4'-chloro-2,3,5,6-tetramethyldiphenyl sulfide

1.2 Other means of identification

Product number -
Other names -

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:77304-54-2 SDS

77304-54-2Downstream Products

77304-54-2Relevant academic research and scientific papers

Lewis Acid Catalyzed Sulphenylation of Methylbenzene by p-Chlorobenzenesulphenyl Chloride

Grant, Douglas W.,Hogg, Donald R.,Wardell, James L.

, p. 3123 - 3143 (2007/10/02)

The Lewis acid catalyzed reactions of benzene and several methylbenzenes with p-chlorobenzenesulphenyl chloride are reported.The products include sulphenylated arenes - p-chlorophenyl aryl sulphides, bis(p-chlorophenylthio)arenes, chloro(p-chlorophenylthio)arenes - as well as chlorinated arenes and bis(p-chlorophenyl)disulphides.The disulphide: combined sulphenylation products ratio for each arene, e.g. 27:73 (for benzene) and 12:86 (for mesitylene), shows only a small variation when compared to the large differences in reactivity of the arenes towards electrophilic reagents.

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