209625-77-4 Usage
Description
(3R,4R)-3,4-DIFLUORO-1-PHENYLPYRROLIDINE is a chiral pyrrolidine derivative with the molecular formula C10H10F2N. It features two fluorine atoms at the 3rd and 4th positions of the pyrrolidine ring and a phenyl group at the 1st position. As a chiral molecule, it exists in two possible stereoisomers, (3R,4R) and (3S,4S). Its unique structure and potential biological activities, such as antiviral and antimicrobial properties, make it a promising candidate for pharmaceutical research and drug development.
Uses
Used in Pharmaceutical Research and Drug Development:
(3R,4R)-3,4-DIFLUORO-1-PHENYLPYRROLIDINE is used as a chemical compound in pharmaceutical research and drug development due to its unique structure and potential biological activities. Its antiviral and antimicrobial properties make it a subject of interest for further scientific investigation and potential drug discovery.
Used in Antiviral Applications:
(3R,4R)-3,4-DIFLUORO-1-PHENYLPYRROLIDINE is used as an antiviral agent for its potential to inhibit viral replication and reduce the severity of viral infections.
Used in Antimicrobial Applications:
(3R,4R)-3,4-DIFLUORO-1-PHENYLPYRROLIDINE is used as an antimicrobial agent for its potential to combat bacterial infections and reduce the spread of antibiotic-resistant bacteria.
Check Digit Verification of cas no
The CAS Registry Mumber 209625-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,6,2 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 209625-77:
(8*2)+(7*0)+(6*9)+(5*6)+(4*2)+(3*5)+(2*7)+(1*7)=144
144 % 10 = 4
So 209625-77-4 is a valid CAS Registry Number.
209625-77-4Relevant articles and documents
Enantioselective syntheses of trans-3,4-difluoropyrrolidines and investigation of their applications in catalytic asymmetric synthesis
Marson, Charles M.,Melling, Robert C.
, p. 9771 - 9779 (2007/10/03)
Asymmetric syntheses of enantiopure trans-3,4-difluoropyrrolidines have been prepared by the introduction of fluorine at both centers in a single operation; asymmetric epoxidations and additions to benzaldehyde were conducted using catalysts whose chirality depends on organofluorine asymmetry.
