321980-62-5 Usage
Uses
Used in Medicinal Chemistry:
1-(4-chlorobenzyl)-2-(trifluoromethyl)-1H-benzo[d]imidazole is used as a chemical intermediate for the development of new drugs. Its unique structure allows it to interact with biological targets and modulate their functions, making it a promising candidate for the treatment of various diseases.
Used in Drug Discovery:
In the field of drug discovery, 1-(4-chlorobenzyl)-2-(trifluoromethyl)-1H-benzo[d]imidazole is used as a lead compound for the identification and optimization of potential therapeutic agents. Its ability to modulate biological targets can lead to the discovery of novel drugs with improved efficacy and safety profiles.
Used in Material Science:
1-(4-chlorobenzyl)-2-(trifluoromethyl)-1H-benzo[d]imidazole is used as a building block in material science for the synthesis of advanced materials with specific properties. Its chemical structure can be tailored to create materials with applications in various industries, such as electronics, aerospace, and automotive.
Used in Organic Synthesis:
In organic synthesis, 1-(4-chlorobenzyl)-2-(trifluoromethyl)-1H-benzo[d]imidazole is used as a key component for the construction of more complex molecules. Its reactivity and functional groups make it a valuable starting material for the synthesis of a wide range of organic compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 321980-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,9,8 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 321980-62:
(8*3)+(7*2)+(6*1)+(5*9)+(4*8)+(3*0)+(2*6)+(1*2)=135
135 % 10 = 5
So 321980-62-5 is a valid CAS Registry Number.
321980-62-5Relevant academic research and scientific papers
Copper-catalyzed tandem C-N bond formation reaction: Selective synthesis of 2-(trifluoromethyl)benzimidazoles
Chen, Mu-Wang,Zhang, Xing-Guo,Zhong, Ping,Hu, Mao-Lin
experimental part, p. 1431 - 1436 (2009/12/08)
A highly practical method for the synthesis of fluorinated benzimidazoles was developed by CuI/TMEDA-catalyzed cross-coupling reaction of N-(2-haloaryl)trifluoroacetimidoyl chlorides with primary amines. The present double amination process tolerates the
