39265-57-1 Usage
Description
(+)-COREY LACTONE, 4-PHENYLBENZOATE ALCOHOL, also known as (3aS,4R,5S,6aR)-Hexahydro-4-(hydroxymethyl)-2-oxo-2H-cyclopenta[b]furan-5-yl Ester [1,1'-Biphenyl]-4-carboxylic Acid, is a corey lactone derivative that serves as a crucial intermediate in the synthesis of prostaglandins. It is a significant compound in the pharmaceutical industry due to its role in the production of essential bioactive molecules.
Uses
Used in Pharmaceutical Industry:
(+)-COREY LACTONE, 4-PHENYLBENZOATE ALCOHOL is used as a key intermediate for the synthesis of prostaglandins, which are essential in various physiological processes and have a wide range of applications in medicine. Prostaglandins are known to play a role in inflammation, pain, and other conditions, making them valuable in the development of therapeutic drugs.
As a key intermediate in the synthesis of prostaglandins, (+)-COREY LACTONE, 4-PHENYLBENZOATE ALCOHOL is crucial for the development of medications that target these physiological processes. Its importance in the pharmaceutical industry lies in its ability to contribute to the creation of drugs that can alleviate pain, reduce inflammation, and address other related health issues.
Check Digit Verification of cas no
The CAS Registry Mumber 39265-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,6 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39265-57:
(7*3)+(6*9)+(5*2)+(4*6)+(3*5)+(2*5)+(1*7)=141
141 % 10 = 1
So 39265-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H20O5/c22-12-17-16-10-20(23)25-18(16)11-19(17)26-21(24)15-8-6-14(7-9-15)13-4-2-1-3-5-13/h1-9,16-19,22H,10-12H2/t16-,17-,18+,19-/m1/s1
39265-57-1Relevant articles and documents
RESOLUTION OF A RACEMIC COREY LACTONE via ENANTIOSELECTIVE ESTERIFICATION
Vesely, Ivan,Palecek, Jaroslav,Stibor, Ivan
, p. 357 - 361 (2007/10/02)
The (-)-enantiomer of Corey lactone Ia has been separated from its (+)-enantiomer Ib via enantioselective esterification of the latter using glycerol tributyrate and a catalytic amount of lipase from Candida cylindracea (EC 3.1.1.3) in an aprotic solvent
11,15-Epiprostaglandin E 2 and its enantiomer. Biological activity and synthesis.
Corey,Terashima,Ramwell,Jessup,Weinshenker,Floyd,Crosby
, p. 3043 - 3044 (2007/10/10)
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