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5,6-Dibromo-1H-benzimidazole is a chemical compound that belongs to the class of organic compounds known as benzimidazoles. Benzimidazoles are compounds containing a benzene ring fused to an imidazole ring, and 5,6-Dibromo-1H-benzimidazole is characterized by the presence of two bromine atoms attached to its benzene ring. It is primarily used in scientific research, particularly in the area of organic chemistry, due to its unique chemical structure and properties. It is generally synthesized in laboratories and isn't naturally occurring. As with many chemical substances, it must be handled with care as it could be potentially harmful if improperly handled.

74545-26-9

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74545-26-9 Usage

Uses

Used in Scientific Research:
5,6-DIBROMO-1H-BENZ(D)IMIDAZOLE is used as a research compound for its unique chemical structure and properties in the field of organic chemistry.
Used in Organic Chemistry:
5,6-DIBROMO-1H-BENZ(D)IMIDAZOLE is used as a synthetic intermediate for the preparation of various organic compounds and derivatives.
Used in Laboratory Synthesis:
5,6-DIBROMO-1H-BENZ(D)IMIDAZOLE is used as a starting material for the synthesis of new compounds in laboratory settings, contributing to the advancement of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 74545-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,4 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74545-26:
(7*7)+(6*4)+(5*5)+(4*4)+(3*5)+(2*2)+(1*6)=139
139 % 10 = 9
So 74545-26-9 is a valid CAS Registry Number.

74545-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Dibromo-1H-benzo[d]imidazole

1.2 Other means of identification

Product number -
Other names 5,6-dibromo-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:74545-26-9 SDS

74545-26-9Downstream Products

74545-26-9Relevant academic research and scientific papers

Visible-light-induced aerobic oxidative desulfurization of 2-mercaptobenzimidazolesviaa sulfinyl radical

Deng, Guo-Jun,Fu, Mei,Huang, Huawen,Ji, Xiaochen,Li, Yongtong

supporting information, p. 5594 - 5598 (2020/09/21)

A mild transition-metal-free non-toxic aerobic photoredox system was found to enable highly efficient desulfurization of 2-mercaptobenzimidazoles. This viable catalytic system includes Rose Bengal in a low catalyst loading as a photosensitizer and cheap, non-toxic NaCl in a catalytic amount as an additive, combined with an oxygen atmosphere. This protocol provides an important alternative access to a broad range of benzimidazole and deuterated benzimidazole products in generally high yields with good tolerance of various synthetically and pharmaceutically useful functionalities. The mechanistic studies reveal that both single electron transfer and energy transfer probably occur in the initial step and a sulfinyl radical intermediate is involved in the key desulfurization process.

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