1021875-67-1 Usage
Uses
Used in Medicinal Chemistry:
(2-AMINO-5-TRIFLUOROMETHYL-3H-IMIDAZOL-4-YL)-PHENYL-METHANONE is used as a building block for the synthesis of new drug candidates, leveraging its unique structure to develop compounds with potential therapeutic applications.
Used in Pharmaceutical Research:
In pharmaceutical research, (2-AMINO-5-TRIFLUOROMETHYL-3H-IMIDAZOL-4-YL)-PHENYL-METHANONE serves as a research tool to study the interactions of small molecules with biological targets, aiding in the understanding of molecular mechanisms and the discovery of novel therapeutic agents.
Used in Drug Development:
(2-AMINO-5-TRIFLUOROMETHYL-3H-IMIDAZOL-4-YL)-PHENYL-METHANONE is utilized in the development of new drugs for the treatment of various diseases and disorders, capitalizing on its potential biological and pharmacological activities to create innovative therapeutic solutions.
Used in Chemical Synthesis:
In the chemical synthesis industry, (2-AMINO-5-TRIFLUOROMETHYL-3H-IMIDAZOL-4-YL)-PHENYL-METHANONE is employed as a key intermediate in the production of complex organic compounds, contributing to the advancement of chemical manufacturing processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1021875-67-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,8,7 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1021875-67:
(9*1)+(8*0)+(7*2)+(6*1)+(5*8)+(4*7)+(3*5)+(2*6)+(1*7)=131
131 % 10 = 1
So 1021875-67-1 is a valid CAS Registry Number.
1021875-67-1Relevant academic research and scientific papers
Synthesis of trifluoromethylated 2-benzoyl- and 2-aminoimidazoles from ring rearrangement of 1,2,4-oxadiazole derivatives
Palumbo Piccionello, Antonio,Pace, Andrea,Buscemi, Silvestre,Vivona, Nicolò,Pani, Marcella
, p. 4004 - 4010 (2008/09/20)
Fluoroalkylated 2-ylamino-imidazoles have been synthesized by reaction of 3-amino-5-phenyl-1,2,4-oxadiazole with fluorinated β-dicarbonyl compounds and subsequent base-induced Boulton-Katritzky Rearrangement (BKR) of the isolated β-enaminocarbonyl interme
