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2-(4-Chlorophenyl)-1H-imidazo(4,5-c)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75007-94-2

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75007-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75007-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,0 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75007-94:
(7*7)+(6*5)+(5*0)+(4*0)+(3*7)+(2*9)+(1*4)=122
122 % 10 = 2
So 75007-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H8ClN3/c13-9-3-1-8(2-4-9)12-15-10-5-6-14-7-11(10)16-12/h1-7H,(H,15,16)

75007-94-2SDS

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 2-(4-chlorophenyl)-3H-imidazo[4,5-c]pyridine

1.2 Other means of identification

Product number -
Other names 2-(4-Chloro-phenyl)-1H-imidazo[4,5-c]pyridine

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:75007-94-2 SDS

75007-94-2Relevant academic research and scientific papers

Na2S2O4: A versatile reagent for the one-pot synthesis of 2-aryl-1h-imidazo[4,5-c]pyridines from 4-amino-3- nitropyridine and aldehydes via reductive cyclization

Dubey,Chowdary,Ramesh,Reddy, P. V. V. Prasada

, p. 697 - 708 (2011/03/19)

A highly efficient and versatile method for the synthesis of 2-aryl-1H-imidazo[4,5-c]pyridines 3 was achieved in one step via reductive cyclization of 4-amino-3-nitro-pyridines 4 with aromatic aldehydes in the presence of Na2S2O

Antiviral 2,5-disubstituted imidazo[4,5-c]pyridines: From anti-pestivirus to anti-hepatitis C virus activity

Puerstinger, Gerhard,Paeshuyse, Jan,De Clercq, Erik,Neyts, Johan

, p. 390 - 393 (2007/10/03)

A novel class of inhibitors of the hepatitis C virus [substituted 2-(2-fluorophenyl)-5H-imidazo[4,5-c]pyridines] is described. Introduction of a fluorine in position 2 of the 2-phenyl substituent of the lead anti-pestivirus compound 1 (5-[(4-bromophenyl)m

VIRAL INHIBITORS

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Page 106-107, (2010/02/06)

The present invention relates to a pharmaceutical composition for the treatment or prevention of viral infections comprising as an active principle at least one imidazo[4,5-c]pyridine derivative having the general formula (Z): (formula). The invention als

Fused imidazoheterocyclic compounds and pharmaceutical compositions

-

, (2008/06/13)

Imidazoheterocyclic compounds having the formula: STR1 wherein the A ring is pyridine in any of its four positions; B is carbonyl, thioxomethyl or hydroxymethylene; Z is hydrogen, halogen, loweralkyl, hydroxy, loweralkoxy, diloweralkylamino or nitro; Ar i

PREPARATION OF 2-ARYL-SUBSTITUTED IMIDAZOPYRIDINES AND IMIDAZOPYRIDINES

Yutilov, Yu. M.,Shcherbina, L. I.

, p. 529 - 535 (2007/10/02)

It is proposed that sulfur be used as the oxidizing agent in the synthesis of 2-arylimidazopyridines from o-diaminopyridines and aromatic (heteroaromatic) aldehydes.Benzyl alcohols and benzylpyridinium salts can be used in place of aldehydes. 2-Phenylimid

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