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62208-53-1

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62208-53-1 Usage

Structure

Benzene ring fused to an imidazole ring, with a diphenylmethyl group attached to the second position of the imidazole ring and a phenyl group attached to the first position.

Type of compound

Benzimidazole derivative

Potential applications

Medicinal chemistry, due to possible pharmacological properties

Use in organic synthesis

Building block, may be of interest in the development of new pharmaceuticals and biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 62208-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,0 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62208-53:
(7*6)+(6*2)+(5*2)+(4*0)+(3*8)+(2*5)+(1*3)=101
101 % 10 = 1
So 62208-53-1 is a valid CAS Registry Number.

62208-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzhydryl-1-phenylbenzimidazole

1.2 Other means of identification

Product number -
Other names 2-benzhydryl-1-phenyl-1H-benzoimidazole

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:62208-53-1 SDS

62208-53-1Downstream Products

62208-53-1Relevant articles and documents

Pd(0)-catalyzed diarylation of sp3 C-H bond in (2-azaaryl)methanes

Song, Guoyong,Su, Yan,Gong, Xue,Han, Keli,Li, Xingwei

supporting information; experimental part, p. 1968 - 1971 (2011/06/25)

A highly efficient and selective palladium-catalyzed diarylation of (2-azaaryl)methanes at the methyl group is described. Aryl chlorides proved reactive enough. A palladium η3-azaallyl intermediate has been identified on the basis of DFT studies.

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