3671-65-6 Usage
Uses
Used in Pharmaceutical Synthesis:
6-Methoxy-2-(trifluoromethyl)benzimidazole is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs for the treatment of certain diseases and conditions.
Used in Organic Chemistry Reactions:
As a building block in organic chemistry, 6-Methoxy-2-(trifluoromethyl)benzimidazole is used in the synthesis of more complex compounds. Its presence in reactions can lead to the formation of novel molecules with potential applications in various industries.
Used in Biological Research:
6-Methoxy-2-(trifluoromethyl)benzimidazole exhibits potential biological activity, making it a valuable compound for research in the field of biology. It may contribute to the discovery of new therapeutic agents or the understanding of biological processes.
Used in Drug Development:
Due to its potential biological activity, 6-Methoxy-2-(trifluoromethyl)benzimidazole is used in the development of new drugs. Its unique structure and properties may offer advantages in the treatment of specific diseases and conditions, providing a promising avenue for pharmaceutical innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 3671-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3671-65:
(6*3)+(5*6)+(4*7)+(3*1)+(2*6)+(1*5)=96
96 % 10 = 6
So 3671-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3N2O/c1-15-5-2-3-6-7(4-5)14-8(13-6)9(10,11)12/h2-4H,1H3,(H,13,14)
3671-65-6Relevant academic research and scientific papers
Rapid one-pot preparation of 2-substituted benzimidazoles from 2-nitroanilines using microwave conditions
VanVliet, David S.,Gillespie, Paul,Scicinski, Jan J.
, p. 6741 - 6743 (2007/10/03)
A high yielding one-pot procedure for the generation of 2-substituted benzimidazoles directly from 2-nitroanilines by in situ reduction and cyclization using a microwave procedure is described.
