1021875-68-2 Usage
Description
1-(2-AMINO-5-METHYL-3H-IMIDAZOL-4-YL)-2,2,2-TRIFLUORO-ETHANONE is a chemical compound characterized by its molecular formula C7H7F3N4O. It is a fluorinated ketone derivative featuring an imidazole ring and an amino group, which contributes to its high reactivity and potential for diverse chemical reactions.
Uses
Used in Pharmaceutical Industry:
1-(2-AMINO-5-METHYL-3H-IMIDAZOL-4-YL)-2,2,2-TRIFLUORO-ETHANONE is used as a building block for the synthesis of various drugs and biologically active molecules due to its unique chemical structure and reactivity.
Used in Organic Synthesis:
1-(2-AMINO-5-METHYL-3H-IMIDAZOL-4-YL)-2,2,2-TRIFLUORO-ETHANONE is also utilized as a reagent in organic synthesis, where its fluorinated ketone and imidazole ring can be employed to create a range of different chemical products.
Used in Chemical Biology:
1-(2-AMINO-5-METHYL-3H-IMIDAZOL-4-YL)-2,2,2-TRIFLUORO-ETHANONE serves as a research tool in chemical biology, where it can be used to study the interactions and mechanisms of various biological systems and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1021875-68-2 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 1021875-68:
(9*1)+(8*0)+(7*2)+(6*1)+(5*8)+(4*7)+(3*5)+(2*6)+(1*8)=132
132 % 10 = 2
So 1021875-68-2 is a valid CAS Registry Number.
1021875-68-2Relevant articles and documents
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
