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16429-33-7

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16429-33-7 Usage

General Description

5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole is a chemical compound with the molecular formula C13H8BrClN2. It is a benzimidazole derivative containing bromine, chlorine, and phenyl groups. 5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole has potential applications in medicinal chemistry due to its structural features and potential biological activities. Benzimidazole derivatives have been reported to have antibacterial, antiviral, antifungal, and anticancer activities, so 5-Bromo-7-chloro-2-phenyl-1H-benzoimidazole may have similar properties. Further research and testing are necessary to fully understand the potential uses and effects of this chemical compound.

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 articles and documents

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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