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97063-37-1

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97063-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97063-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,6 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97063-37:
(7*9)+(6*7)+(5*0)+(4*6)+(3*3)+(2*3)+(1*7)=151
151 % 10 = 1
So 97063-37-1 is a valid CAS Registry Number.

97063-37-1SDS

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 1-chloro-2-[1-(2-chlorophenyl)ethenyl]benzene

1.2 Other means of identification

Product number -
Other names 1,1-Bis-(2-chlorphenyl)-ethylen

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:97063-37-1 SDS

97063-37-1Downstream Products

97063-37-1Relevant articles and documents

HIGH-TEMPERATURE ORGANIC SYNTHESIS. XXII. THERMAL TRANSFORMATIONS OF EXO-CHLORINE-SUBSTITUTED TOLUENES

Voronkov, M. G.,Deryagina, E. N.,Shagun, L. G.,Vitkovskii, V. Yu.

, p. 962 - 966 (2007/10/02)

The gas-phase pyrolysis of exo-chlorine-substituted toluenes in an atmosphere of nitrogen or hydrogen sulfide was investigated.Hydrogen sulfide stimulates the thermolysis of benzyl chloride, accelerating the formation of toluene and stilbene at 430 deg C.The other reaction products are anthracene and bibenzyl.Similar compounds and also phenanthrene are formed during the pyrolysis of benzylidene chloride in an atmosphere of nitrogen or hydrogen sulfide (500 deg C).Benzotrichloride is distinguished by its high stability; its pyrolysis mainly with the formation of 1,2-dichloro-1,2-diphenylethylene is realized at temperatures above 550 deg C.With hydrogen sulfide it reacts at 400 deg C to form bibenzyl, stilbene, anthracene, phenanthrene, and thianaphtenothianaphthene.The latter is the main product in a recirculation-type system.

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