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1,4-Cyclohexadiene, 1-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95309-13-0

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95309-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95309-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,0 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95309-13:
(7*9)+(6*5)+(5*3)+(4*0)+(3*9)+(2*1)+(1*3)=140
140 % 10 = 0
So 95309-13-0 is a valid CAS Registry Number.

95309-13-0SDS

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-chlorocyclohexa-1,4-diene

1.2 Other means of identification

Product number -
Other names 1-Chlor-cyclohexa-1,4-dien

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:95309-13-0 SDS

95309-13-0Relevant academic research and scientific papers

The Free Radical Reaction between Alkanes and Carbon Tetrachloride

Hawari, J. A.,Davis, S.,Engel, P. S.,Gilbert, B. C.,Griller, D.

, p. 4721 - 4724 (1985)

Product studies and kinetic electron paramagnetic resonance methods were used to investigate the free radical reaction between alkanes and carbon tetrachloride in solution.Trichloromethyl radicals abstracted hydrogen from simple alkanes with rate constants of ca. 60 M-1 s-1 at 300 K. in good agreement with gas-phase data.However, rate constants for chlorine abstraction by alkyl radicals from carbon tetrachloride were ca.E4 M-1 s-1 and were therefore ca. 2 orders of magnitude higher in solution than in the gas phase.Possibilities for the origin of this effect are discussed.

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