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5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole is a chemical compound with the molecular formula C13H8BrClN2. It is a benzimidazole derivative that incorporates bromine, chlorine, and phenyl groups, which may contribute to its potential biological activities and applications in medicinal chemistry.

16429-33-7

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16429-33-7 Usage

Uses

Used in Medicinal Chemistry:
5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole is used as a potential candidate for the development of new drugs due to its structural features and the known biological activities of benzimidazole derivatives. These activities include antibacterial, antiviral, antifungal, and anticancer properties, which make it a promising compound for further research and testing in the pharmaceutical industry.
Used in Antibacterial Applications:
In the field of antibacterial research, 5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole is used as a potential antibacterial agent, leveraging the broad-spectrum antimicrobial properties often associated with benzimidazole derivatives.
Used in Antiviral Applications:
5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole is used as a potential antiviral agent, given the antiviral activities that have been reported for some benzimidazole compounds, which could be beneficial in combating viral infections.
Used in Antifungal Applications:
In antifungal research, 5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole is used as a potential antifungal agent, building on the known antifungal capabilities of benzimidazole derivatives to treat fungal infections.
Used in Anticancer Applications:
5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole is used as a potential anticancer agent, with the aim of exploiting its possible cytotoxic effects on cancer cells, which is a common characteristic of certain benzimidazole compounds.
Further research and testing are necessary to fully understand the potential uses and effects of 5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole, as its exact applications and mechanisms of action may vary depending on the specific context and conditions of use.

Check Digit Verification of cas no

The CAS Registry Mumber 16429-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,2 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16429-33:
(7*1)+(6*6)+(5*4)+(4*2)+(3*9)+(2*3)+(1*3)=107
107 % 10 = 7
So 16429-33-7 is a valid CAS Registry Number.

16429-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-4-chloro-2-phenyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-Phenyl-5-brom-7-chlorbenzimidazol

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:16429-33-7 SDS

16429-33-7Downstream Products

16429-33-7Relevant academic research and scientific papers

Visible light promoted tandem dehydrogenation-deaminative cyclocondensation under aerobic conditions for the synthesis of 2-aryl benzimidazoles/quinoxalines fromortho-phenylenediamines and arylmethyl/ethyl amines

Sofi, Firdoos Ahmad,Sharma, Rohit,Rawat, Ravi,Chakraborti, Asit K.,Bharatam, Prasad V.

supporting information, p. 4569 - 4573 (2021/03/22)

Visible light promoted domino synthesis of 2-aryl benzimidazoles is reported through the reaction ofortho-phenylenediamines and arylmethyl amines under aerobic conditions. The methodology has wide substrate scope and tolerates a wide range of functional groups affording the products in high yields. The use of arylethyl amines instead of arylmethyl amines gives 2-aryl quinoxalines.

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