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1H-Benzimidazole-6-carbonitrile,1-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53484-14-3

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53484-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53484-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,8 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53484-14:
(7*5)+(6*3)+(5*4)+(4*8)+(3*4)+(2*1)+(1*4)=123
123 % 10 = 3
So 53484-14-3 is a valid CAS Registry Number.

53484-14-3SDS

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 3-methylbenzimidazole-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 1h-benzimidazole-6-carbonitrile,1-methyl

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:53484-14-3 SDS

53484-14-3Relevant academic research and scientific papers

Cu-Catalyzed C-H Allylation of Benzimidazoles with Allenes

Dong, Yaxi,Breit, Bernhard

supporting information, p. 6765 - 6769 (2021/09/11)

CuH-catalyzed intramolecular cyclization and intermolecular allylation of benzimidazoles with allenes have been described. The reaction proceeded smoothly with the catalytic system of Cu(OAc)2/Xantphos and catalytic amount of (MeO)2MeSiH. This protocol features mild reaction conditions and a good tolerance of substrates bearing electron-withdrawing, electron-donating, or electron-neutral groups. A new catalytic mechanism was proposed for this copper hydride catalytic system.

THIAZOLONES FOR USE AS PI3 KINASE INHIBITORS

-

, (2008/06/13)

Invented is a method of inhibiting the activity/function of PI3 kinases using substituted thiazolones. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, ne

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