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5-CHLORO-1,2-DIMETHYLBENZIMIDAZOLE is a chemical compound with the molecular formula C9H9ClN2, belonging to the benzimidazole class of compounds. It features a chloro substituent at the 5-position and two methyl groups at the 1 and 2 positions, which contribute to its unique chemical properties and potential applications.

26960-04-3

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26960-04-3 Usage

Uses

Used in Pharmaceutical Synthesis:
5-CHLORO-1,2-DIMETHYLBENZIMIDAZOLE is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules, enhancing their therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, 5-CHLORO-1,2-DIMETHYLBENZIMIDAZOLE is utilized as an intermediate in the production of agrochemicals, potentially contributing to the development of new pesticides or herbicides.
Used in Antifungal and Antimicrobial Applications:
5-CHLORO-1,2-DIMETHYLBENZIMIDAZOLE is studied for its potential antifungal and antimicrobial properties, making it a candidate for use in treatments or products that combat fungal and microbial infections.
Used as a Corrosion Inhibitor:
This chemical has been investigated for its potential use as a corrosion inhibitor, which could be applied in industries where materials are prone to corrosion, thus extending the lifespan of equipment and structures.
Used in Materials Science:
5-CHLORO-1,2-DIMETHYLBENZIMIDAZOLE is considered as a building block for the synthesis of heterocyclic compounds, which are important in materials science for their diverse applications, including the development of new materials with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 26960-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,6 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26960-04:
(7*2)+(6*6)+(5*9)+(4*6)+(3*0)+(2*0)+(1*4)=123
123 % 10 = 3
So 26960-04-3 is a valid CAS Registry Number.

26960-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-1,2-dimethylbenzimidazole

1.2 Other means of identification

Product number -
Other names 5-Chlor-1,2-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:26960-04-3 SDS

26960-04-3Relevant academic research and scientific papers

Design and synthesis of 3-(benzimidazol-2-yl)-propionic acids as thromboxane A2 receptor antagonists

Garuti,Ghedini,Leoni,Baraldi,Dionisotti

, p. 1531 - 1546 (2007/10/02)

A series of 3-(benzimidazol-2-yl)-propionic acids substituted at the N1 nitrogen with methyl and benzyl groups and at the C5 and C6 positions with chloro, methoxy, amino, hydroxyl groups were synthesized and tested as TXA2 receptor antagonists.

Condensation of o-Diamines with Dehydroacetic Acid and Pyrolysis of Resultant Products

Qayyoom, M. A.,Hanumanthu, P.,Ratnam, C. V

, p. 883 - 884 (2007/10/02)

Condensation of o-phenylenediamines with dehydroacetic acid (I) yields 3--4-hydroxy-6-methyl-2(H)-pyrones (II), which on pyrolysis give the corresponding 2-methylbenzimidazoles (V).

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