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17583-45-8

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17583-45-8 Usage

Structure

A heterocyclic aromatic organic compound derived from benzimidazole.

Usage

Commonly used in the synthesis of organic compounds and pharmaceuticals.

Reactivity

Diverse reactivity due to its chemical structure.

Biological Activity

Possesses potential biological activity.

Applications

Medicinal chemistry, drug development, agriculture, and industrial processes.

Structural Features

Contains two methyl groups at the 1st and 7th positions of the benzimidazole ring.

Pharmacological Properties

Has potential pharmacological properties that contribute to its applications in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 17583-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,8 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17583-45:
(7*1)+(6*7)+(5*5)+(4*8)+(3*3)+(2*4)+(1*5)=128
128 % 10 = 8
So 17583-45-8 is a valid CAS Registry Number.

17583-45-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-dimethyl-1H-benzo[d]imidazole

1.2 Other means of identification

Product number -
Other names 1,7-Dimethyl-1H-benzimidazol

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:17583-45-8 SDS

17583-45-8Downstream Products

17583-45-8Relevant articles and documents

Development of a regioselective N-methylation of (benz)imidazoles providing the more sterically hindered isomer

Van Den Berge, Emilie,Robiette, Raphael

, p. 12220 - 12223 (2013)

An efficient and highly regioselective N-methylation of (NH)-(benz)imidazoles furnishing the sterically more hindered, less stable, and usually minor regioisomer has been developed. The methodology involves very mild reaction conditions and tolerates a wide range of functional groups.

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