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2-Benzimidazolecarbonitrile,5-fluoro-(8CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29958-83-6

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29958-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29958-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,5 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29958-83:
(7*2)+(6*9)+(5*9)+(4*5)+(3*8)+(2*8)+(1*3)=176
176 % 10 = 6
So 29958-83-6 is a valid CAS Registry Number.

29958-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-1H-benzimidazole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-ethyl-pyridine-2-carbonitrile

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:29958-83-6 SDS

29958-83-6Downstream Products

29958-83-6Relevant academic research and scientific papers

Synthesis of novel histamine H4 receptor antagonists

Lane, Charlotte A.L.,Hay, Duncan,Mowbray, Charles E.,Paradowski, Michael,Selby, Matthew D.,Swain, Nigel A.,Williams, David H.

scheme or table, p. 1156 - 1159 (2012/03/11)

This letter describes the discovery and synthesis of a series of octahydropyrrolo[3,4-c]pyrrole based selective histamine hH4 receptor antagonists. The amidine compound 20 was found to be a potent and selective histamine H4 receptor antagonist with moderate clearance and a high volume of distribution.

1,2,4-OXADIAZOLE SUBSTITUTED PIPERIDINE AND PIPERAZINE DERIVATIVES AS SMO ANTAGONISTS

-

Page/Page column 67-68, (2010/04/03)

The present invention relates to compounds of formula (I): and pharmaceutically acceptable salts, stereoisomers or tautomers thereof which are inhibitors of the Sonic Hedgehog pathway, in particular Smo antagonists. Thus the compounds of this invention are useful for the treatment of diseases associated with abnormal hedgehog pathway activation, including cancer, for example basal cell carcinoma, medulloblastoma, prostate, pancreatic, breast, colon, bone and small cell lung cancers, and cancers of the upper GI tract.

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