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1H-Benzimidazole, 1-(4-chlorophenyl)-2-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24784-42-7

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24784-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24784-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,8 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24784-42:
(7*2)+(6*4)+(5*7)+(4*8)+(3*4)+(2*4)+(1*2)=127
127 % 10 = 7
So 24784-42-7 is a valid CAS Registry Number.

24784-42-7Downstream Products

24784-42-7Relevant academic research and scientific papers

Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2-arylation/heteroarylation of N-substituted benzimidazoles

Gokanapalli, Anusha,Motakatla, Venkata Krishna Reddy,Peddiahgari, Vasu Govardhana Reddy

, (2020/07/06)

A convenient and highly efficient palladium-catalyzed direct C2-arylation/heteroarylation of N-substituted benzimidazole derivatives such as N-benzyl/3-chlorobenzyl/2,4,6-trimethylbenzyl/2,4,6-triisopropylbenzyl/aryl benzimidazoles with various aryl/heter

Discovery of new leads against Mycobacterium tuberculosis using scaffold hopping and shape based similarity

Wavhale, Ravindra D.,Martis, Elvis A.F.,Ambre, Premlata K.,Wan, Baojie,Franzblau, Scott G.,Iyer, Krishna R.,Raikuvar, Kavita,Macegoniuk, Katarzyna,Berlicki, ?ukasz,Nandan, Santosh R.,Coutinho, Evans C.

, (2017/10/06)

BM212 [1,5-diaryl-2-methyl-3-(4-methylpiperazin-1-yl)-methyl-pyrrole] is a pyrrole derivative with strong inhibitory activity against drug resistant Mycobacterium tuberculosis and mycobacteria residing in macrophages. However, it was not pursued because o

One-pot sequential synthesis of 1,2-disubstituted benzimidazoles under metal-free conditions

Roy, Priyabrata,Pramanik, Animesh

supporting information, p. 5243 - 5245 (2013/09/02)

An easy and inexpensive method has been developed to access 1,2-disubstituted benzimidazoles following a one-pot sequential coupling/reduction/cyclization process under metal-free neutral conditions.

Methods of treating or preventing interstitial cystitis

-

, (2008/06/13)

PCT No. PCT/US97/03895 Sec. 371 Date Aug. 25, 1998 Sec. 102(e) Date Aug. 25, 1998 PCT Filed Mar. 7, 1997 PCT Pub. No. WO97/33873 PCT Pub. Date Sep. 18, 1997This invention provides methods for the treatment or prevention of interstitial cystitis or urethral syndrome in a mammal which comprise administering to a mammal in need thereof an effective amount of a substituted benzimidazole, or a pharmaceutically acceptable salt or solvate thereof.

Methods of treating or preventing sleep apnea

-

, (2008/06/13)

This invention provides methods for the treatment or prevention of sleep apnea in a mammal which compris administering to a mammal in need thereof an effective amount of a substituted benzimidazole, or a pharmaceutically acceptable salt or solvate thereof.

METHODS FOR TREATING A PHYSIOLOGICAL DISORDER ASSOCIATED WITH BETA-AMYLOID PEPTIDE

-

, (2008/06/13)

This invention provides substituted benzimidazoles which are useful in treating or preventing conditions associated with beta-amyloid peptide. Some such conditions associated with beta-amyloid peptide include Alzheimer's Disease, Down's Symdrome and amyloidosis of the Dutch type

Non-peptidyl tachykinin receptor antagonists

-

, (2008/06/13)

This invention provides novel substituted benzimidazoles of formula II which are useful as tachykinin receptor antagonists. This invention also provides methods for treating a condition associated with an excess of tachykinin which comprises administering to a mammal in need thereof one of a series of substituted benzimidazoles. This invention further provides pharmaceutical formulations comprising one or more of the substituted benzimidazoles of the present invention in association with pharmaceutical carriers, diluents, or excipients. A and Ra-Re are as defined in the description.

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