209679-20-9 Usage
Uses
Used in Pharmaceutical Research and Development:
(S)-3-(4-FLUOROPHENYL)BUTANOIC ACID is utilized as a building block in the synthesis of various drugs and pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new therapeutic agents.
Used in Drug-Receptor Interaction Studies:
(S)-3-(4-FLUOROPHENYL)BUTANOIC ACID is employed as a tool in the study of drug-receptor interactions, helping researchers understand how different drugs bind to their target receptors and exert their therapeutic effects.
Used in Drug Metabolism Research:
(S)-3-(4-FLUOROPHENYL)BUTANOIC ACID is used in the investigation of drug metabolism, providing insights into how drugs are processed and eliminated from the body, which is crucial for optimizing drug efficacy and safety.
Used in Anti-Inflammatory Applications:
(S)-3-(4-FLUOROPHENYL)BUTANOIC ACID is used as an anti-inflammatory agent, potentially reducing inflammation and alleviating symptoms associated with various inflammatory conditions.
Used in Neuroprotective Applications:
As a neuroprotective agent, (S)-3-(4-FLUOROPHENYL)BUTANOIC ACID may help protect neurons from damage or degeneration, offering potential benefits in the treatment of neurodegenerative diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 209679-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,6,7 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 209679-20:
(8*2)+(7*0)+(6*9)+(5*6)+(4*7)+(3*9)+(2*2)+(1*0)=159
159 % 10 = 9
So 209679-20-9 is a valid CAS Registry Number.
209679-20-9Relevant articles and documents
Lipase catalysed kinetic resolutions of 3-aryl alkanoic acids
Deasy, Rebecca E.,Brossat, Maude,Moody, Thomas S.,Maguire, Anita R.
, p. 47 - 61 (2011/04/18)
Hydrolase catalysed kinetic resolutions leading to a series of 3-aryl alkanoic acids (≥94% ee) are described. Hydrolysis of the ethyl esters with a series of hydrolases was undertaken to identify biocatalysts that yield the corresponding acids with excellent enantiopurity in each case. Steric and electronic effects on the efficiency and enantioselectivity of the biocatalytic transformation were also explored.
