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1H-Benzimidazole, 1-(4-bromophenyl)-2-ethyl-, also known as 1-(4-bromophenyl)-2-ethyl-1H-benzimidazole, is a chemical compound with the molecular formula C15H13BrN2. It belongs to the class of benzimidazoles, which are heterocyclic compounds containing a benzene ring fused to an imidazole ring. 1H-Benzimidazole, 1-(4-bromophenyl)-2-ethylis characterized by the presence of a bromine atom attached to the phenyl group and an ethyl group at the 2nd position of the benzimidazole core. It is known for its potential therapeutic and biological activities, making it a valuable compound in the synthesis of pharmaceuticals and agrochemicals.

97870-64-9

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97870-64-9 Usage

Uses

Used in Pharmaceutical Industry:
1H-Benzimidazole, 1-(4-bromophenyl)-2-ethylis used as a key intermediate in the synthesis of various pharmaceuticals for its potential therapeutic properties. Its unique structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 1H-Benzimidazole, 1-(4-bromophenyl)-2-ethylis utilized in the synthesis of agrochemicals, such as pesticides and fungicides, due to its potential biological activities. Its ability to inhibit enzyme function and exhibit antifungal properties makes it a valuable component in the development of effective crop protection agents.
Used in Anticancer Research:
1H-Benzimidazole, 1-(4-bromophenyl)-2-ethylis used as an anticancer agent in research settings. Its potential to inhibit enzyme function and exhibit anticancer properties has led to investigations into its use as a therapeutic agent against various types of cancer. Further research is needed to fully understand its mechanism of action and optimize its potential as a cancer treatment.
Used in Chemical Biology and Medicinal Chemistry Research:
As a chemical compound with unique structural features and potential biological activities, 1H-Benzimidazole, 1-(4-bromophenyl)-2-ethylserves as a valuable tool in chemical biology and medicinal chemistry research. It can be used to probe the structure-activity relationships of various biological targets, aiding in the discovery of novel therapeutic agents and deepening our understanding of biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 97870-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,7 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 97870-64:
(7*9)+(6*7)+(5*8)+(4*7)+(3*0)+(2*6)+(1*4)=189
189 % 10 = 9
So 97870-64-9 is a valid CAS Registry Number.

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