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1,2-Diphenyl-1H-imidazo[1,2-a]benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36289-17-5

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36289-17-5 Usage

Type of compound

Benzimidazole derivative

Usage

Research and development in the pharmaceutical industry

Properties

Anti-cancer potential, inhibits growth of certain cancer cells

Application

Building block for the synthesis of various organic compounds

Physical state

Solid, crystalline structure

Handling and storage

Controlled laboratory environment, safety protocols followed

Check Digit Verification of cas no

The CAS Registry Mumber 36289-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,8 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36289-17:
(7*3)+(6*6)+(5*2)+(4*8)+(3*9)+(2*1)+(1*7)=135
135 % 10 = 5
So 36289-17-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H15N3/c1-3-9-16(10-4-1)20-15-23-19-14-8-7-13-18(19)22-21(23)24(20)17-11-5-2-6-12-17/h1-15H

36289-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Diphenyl-1H-imidazo[1,2-a]benzimidazole

1.2 Other means of identification

Product number -
Other names 1,2-diphenyl-1-cyclopropene

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:36289-17-5 SDS

36289-17-5Relevant academic research and scientific papers

1-Acylmethylbenzimidazole-2-sulfonic acids and their cyclization by N-nucleophiles

Kuz'Menko,Divaeva,Morkovnik,Anisimova,Borodkin,Kuz'Menko

, p. 716 - 724 (2014/07/08)

New preparation method was developed for derivatives of 1,4-dihydro-1,2,4-triazino[4,3-a]-, 2-aryl-1(9)H-, and 1-R-imidazo[1,2-a] benzimidazole underlain by newly synthesized 1-acylmethylbenzimidazole-2- sulfonic acids. The latter react with 2-aminoethanol affording along with the previously described compounds of the 1-(2-hydroxyethyl)imidazobenzimidazole series also compounds of formerly unknown polycyclic system, 2,3,11,12-tetrahydro-1,3-oxazolo[2,3-a]imidazo[1,2-a]benzimidazole.

1,2-DIPHENYLIMIDAZOBENZIMIDAZOLEIN ELECTROPHILIC SUBSTITUTION REACTIONS

Priimenko, B. A.,Klyuev, N. A.,Sapozhnikov, Yu. M.,Garmash, S. N.,Kochrgin, P. M.

, p. 937 - 940 (2007/10/02)

Vilsmeier formylation of 1,2-diphenylimidazobenzimidazole leads to the 3-formyl derivative, while heating with acetic anhydride in sulfuric acid gives the 3-acetyl derivative.The nitration of this benzimidazole with potassium nitrate in sulfuric ac

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