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96436-29-2

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96436-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96436-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,3 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96436-29:
(7*9)+(6*6)+(5*4)+(4*3)+(3*6)+(2*2)+(1*9)=162
162 % 10 = 2
So 96436-29-2 is a valid CAS Registry Number.

96436-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,6-dimethylbenzoyl) 2,6-dimethylbenzenecarboperoxoate

1.2 Other means of identification

Product number -
Other names Peroxide,bis(2,6-dimethylbenzoyl)

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:96436-29-2 SDS

96436-29-2Upstream product

96436-29-2Relevant articles and documents

Structural and Solvent Effects upon Decarboxylation of 2,6-Disubstituted Benzoyloxyl Radicals. A Laser Flash Photolysis Study of Bis(2,6-disubstituted-benzoyl) Peroxides

Wang, Jun,Itoh, Hiroki,Tsuchiya, Masahiro,Tokumaru, Katsumi,Sakuragi, Hirochika

, p. 11967 - 11978 (1995)

The rate constants for decarboxylation of 2,6-dimethylbenzoyloxyl, 2,4,6-trimethylbenzoyloxyl and 2,6-dichlorobenzoyloxyl radicals are larger than those of benzoyloxyl, 4-methylbenzoyloxyl and 2-chlorobenzoyloxyl radicals, respectively, in carbon tetrachloride and acetonitrile; however, the values in the former solvent are significantly larger than those in the latter.The rate acceleration with the ortho substituents is ascribed to a nonplanar geometry of the radicals brought about by twisting of the carbonyloxyl group due to a steric effect of the substituents.The polar solvent serves to stabilize a twisted charge-transfer structure of the radicals and retards their decarboxylation.

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