1020717-92-3 Usage
Appearance
White solid at room temperature the compound appears as a white solid in its pure form when it is at normal temperature conditions.
Usage as an intermediate
Synthesis of pharmaceuticals and agrochemicals 1-PHENYL-5-TRIFLUOROMETHYL-PYRROLIDIN-2-ONE is commonly used as a starting material or intermediate in the production of various drugs and agricultural chemicals.
Biological activities
Antioxidant and anti-inflammatory properties the compound has the potential to neutralize harmful free radicals and reduce inflammation in biological systems.
Building block in organic synthesis
Reactivity and versatility due to its chemical structure and properties, 1-PHENYL-5-TRIFLUOROMETHYL-PYRROLIDIN-2-ONE can be used as a component in the creation of a wide range of other organic compounds.
Chiral auxiliary potential
Asymmetric synthesis of chiral compounds 1-PHENYL-5-TRIFLUOROMETHYL-PYRROLIDIN-2-ONE has been studied for its possible use in helping to create chiral compounds (molecules with non-superimposable mirror images) in an asymmetric manner, which is important in the production of many drugs and other fine chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1020717-92-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,7,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1020717-92:
(9*1)+(8*0)+(7*2)+(6*0)+(5*7)+(4*1)+(3*7)+(2*9)+(1*2)=103
103 % 10 = 3
So 1020717-92-3 is a valid CAS Registry Number.
1020717-92-3Relevant articles and documents
Reductive amination/cyclization of ω-trifluoromethyl keto esters to trifluoromethylated δ-amino alcohols and lactams
Wan, Wen,Hou, Jie,Jiang, Haizhen,Yuan, Zongqian,Goubin, Ma.,Zhao, Gang,Hao, Jian
experimental part, p. 1778 - 1786 (2010/06/15)
A reductive amination/cyclization approach towards biologically interesting trifluoromethylated four- to seven-membered ring lactams from simply prepared ω-trifluoromethyl keto esters in good to excellent yields has been developed. In addition, trifluorom
