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6-methyl-1,2-diphenyl-1H-benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86318-02-7

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86318-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86318-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,1 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86318-02:
(7*8)+(6*6)+(5*3)+(4*1)+(3*8)+(2*0)+(1*2)=137
137 % 10 = 7
So 86318-02-7 is a valid CAS Registry Number.

86318-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-1,2-diphenyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 6-Methyl-1,2-diphenylbenzimidazol

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:86318-02-7 SDS

86318-02-7Relevant academic research and scientific papers

Copper-catalyzed synthesis of 1,2-disubstituted benzimidazoles from imidoyl chlorides

Yu, Hui,Zhang, Mei Shu,Cui, Li Ren

experimental part, p. 573 - 575 (2012/07/14)

A strategy for the synthesis of 1,2-disubstituted benzimidazoles has been developed and a variety of 1,2-disubstituted benzimidazoles were obtained from imidoyl chlorides and o-haloanilines via copper(I)-catalyzed reaction in moderate yields.

Reactivity-controlled regioselectivity: A regiospecific synthesis of 1,2-disubstituted benzimidazoles

Deng, Xiaohu,Mani, Neelakandha S.

experimental part, p. 680 - 686 (2010/03/04)

We demonstrate exceptional levels of regioselectivity in the tandem, animation reactions between 1,2-differentiated dihaloarenes and N-substituted amidines, The regiochemical outcome of this Cul-catalyzed reaction is achieved through a combination of N1/N2 chemoselectivity on the amidine and reactivity-controlled X1/X2 chemoselectivity on the 1,2-dihaloarene. This reaction proves to be fairly general for the regiospecific synthesis of 1,2-substituted benzimidazoles.

1,2 diarylbenzimdazoles and their pharmaceutical use

-

, (2008/06/13)

Benzimidazoles of general formula I and the use of benzimidazole derivatives for the production of pharmaceutical agents for treatment and prophylaxis of diseases that are associated with a microglia activation are described.

Memory Effects and 1,3-Diazepine Ring Closure in Arylnitrenium Ions

Binding, Norbert,Heesing, Albert

, p. 1822 - 1833 (2007/10/02)

15N- and 18O-Labelling experiments demonstrate that in the aromatic rearrangement of N,N'-diphenyl-N-(4-tosyloxy)benzamidines (2 -> 3 - 6) a strong memory effect occurs in oriented contact ion pairs.The formation of 1,3-diazepines 9 by ring closure betwee

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