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60750-02-9

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60750-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60750-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,5 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60750-02:
(7*6)+(6*0)+(5*7)+(4*5)+(3*0)+(2*0)+(1*2)=99
99 % 10 = 9
So 60750-02-9 is a valid CAS Registry Number.

60750-02-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-5-phenyl-2-(4-phenylphenyl)pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2-[1,1'-biphenyl]-4-yl-4-methyl-5-phenyl

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:60750-02-9 SDS

60750-02-9Downstream Products

60750-02-9Relevant articles and documents

The Decomposition Kinetics of Benzoyl Peroxide in Pyridine and in Pyridine-Benzene

Vidal, Simone,Court, Jean,Bonnier, Jane-Marie

, p. 663 - 668 (2007/10/02)

The decomposition kinetics of benzoyl peroxide in pyridine and in pyridine-benzene have been studied in the presence and absence of an inhibitor.We observed that pyridine could induce the decomposition of benzoyl peroxide, the reaction of which was first-order with respect to the peroxide and pyridine, respectively, to give pyridine N-oxide and benzoic anhydride.We demonstrated that pyridine cation radicals are not formed in the reaction.The unusual decrease of the first-order rate constant for the decomposition of benzoyl peroxide in pyridine with the increase of the initial concentration is ascribed to a decomposition induced by the dihydro- and tetrahydro pyridines which predominates at low initial concentrations.

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