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261710-03-6

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261710-03-6 Usage

Derivative of benzimidazole

A heterocyclic aromatic organic compound, which serves as the base structure for this chemical compound.

Amine group present

The presence of an amine group (-NH2) contributes to the compound's basic properties and potential applications in chemical and pharmaceutical industries.

Nitro group present

The presence of a nitro group (-NO2) suggests that the compound may have potential as a precursor or intermediate in the synthesis of other compounds.

Potential applications

The compound's specific properties and potential uses would depend on further testing and research within the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 261710-03-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,7,1 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 261710-03:
(8*2)+(7*6)+(6*1)+(5*7)+(4*1)+(3*0)+(2*0)+(1*3)=106
106 % 10 = 6
So 261710-03-6 is a valid CAS Registry Number.

261710-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitrobenzimidazol-1-amine

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazol-1-amine,5-nitro

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:261710-03-6 SDS

261710-03-6Upstream product

261710-03-6Downstream Products

261710-03-6Relevant articles and documents

Reactions of a series of 1-aminobenzimidazoles and 1-amino-3- methylbenzimidazolium chlorides with 2,4-pentanedione

Kaiya, Toyo,Aoyama, Shinsuke,Kohda, Kohfuku

, p. 37 - 42 (2007/10/03)

Reactions of a series of 1-aminobenzimidazoles and 1-amino-3- methylbenzimidazolium chlorides with 2,4-pentanedione were carried out and pyridazino[1,6-a]benzimidazoles and 2-pyrazolylanilines were generated. The product ratios of these compounds remarkably depended on the reaction conditions and on the electronic character of the substituent at the benzene moiety. The possible mechanisms involved in these reactions are discussed. (C) 2000 Elsevier Science Ltd.

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