209625-77-4 Usage
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 academic research and scientific papers
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.
The first enantioselective syntheses of vicinal difluoropyrrolidines and the first catalytic asymmetric synthesis mediated by the C2 symmetry of a -CHFCHF- Unit
Marson, Charles M.,Melling, Robert C.
, p. 1223 - 1224 (2007/10/03)
The first enantiopure vicinal difluorides of C2 symmetry have been prepared by the introduction of fluorine at both centres in a single operation; the first asymmetric synthesis using a catalyst whose chirality depends on organofluorine asymmetry is described.
