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1H-Benzimidazole,4-chloro-2-methyl-(9CI) is a chemical compound belonging to the benzimidazole class, characterized by the molecular formula C9H7ClN2. It features a chlorine atom and a methyl group attached to the benzimidazole ring, which may contribute to its diverse biological activities.

5599-82-6

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5599-82-6 Usage

Uses

Used in Pharmaceutical Industry:
1H-Benzimidazole,4-chloro-2-methyl-(9CI) is used as a potential pharmaceutical candidate due to its benzimidazole class, which is known for exhibiting antiparasitic, antimicrobial, and anticancer properties. Further research is required to fully understand its specific properties and potential applications in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 5599-82-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,9 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5599-82:
(6*5)+(5*5)+(4*9)+(3*9)+(2*8)+(1*2)=136
136 % 10 = 6
So 5599-82-6 is a valid CAS Registry Number.

5599-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2-methyl-1H-benzo[d]imidazole

1.2 Other means of identification

Product number -
Other names 4-chloro-2-methyl-1H-benzimidazole

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:5599-82-6 SDS

5599-82-6Downstream Products

5599-82-6Relevant academic research and scientific papers

BF3·Et2O promoted one-pot expeditious and convenient synthesis of 2-substituted benzimidazoles and 3,1,5-benzoxadiazepines

Tandon, Vishnu K.,Kumar, Manoj

, p. 4185 - 4187 (2007/10/03)

2-Substituted benzimidazoles and 3,1,5-benzoxadiazepines have been synthesized in excellent yields in a single pot by cyclodehydration of N-acyl-1,2-phenylenediamines and N,N′-diacyl-1,2- phenylenediamines prepared in situ from the corresponding 1,2-phenylenediamines and an acid chloride, respectively.

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