5062-62-4 Usage
Uses
Used in Pharmaceutical Industry:
20-Dihydroprogesterone Acetate is used as a pharmaceutical compound for its potential applications in cardiovascular and menopausal studies. As an analogue of progesterone, it may have similar effects on the human body, making it a valuable candidate for research and development in these areas.
Used in Research and Development:
20-Dihydroprogesterone Acetate is used as a research compound to study the effects of progesterone and its analogues on various physiological processes. This can help in understanding the role of progesterone in the body and developing new treatments for related conditions.
Used in Hormone Replacement Therapy:
Although not explicitly mentioned in the provided materials, 20-Dihydroprogesterone Acetate, due to its similarity to progesterone, could potentially be used in hormone replacement therapy for menopausal women. This application would be based on the compound's ability to mimic the effects of natural progesterone in the body.
Check Digit Verification of cas no
The CAS Registry Mumber 5062-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5062-62:
(6*5)+(5*0)+(4*6)+(3*2)+(2*6)+(1*2)=74
74 % 10 = 4
So 5062-62-4 is a valid CAS Registry Number.
5062-62-4Relevant academic research and scientific papers
Regioselective esterification of polyhydroxylated steroids by Candida antarctica lipase B
Bertinotti, Anna,Carrea, Giacomo,Ottolina, Gianluca,Riva, Sergio
, p. 13165 - 13172 (2007/10/02)
The regioselectivity of Candida antarctica lipase B towards the acetylation of polyhydroxylated steroids has been systematically investigated. The enzyme showed a marked preference for the alcoholic moieties on the A ring and: on the steroidal side chain, making it possible the selective acylation at the positions 3 or 21 of polyhydroxy steroids. Acylation with the synthetically useful esters chloroacetate and levulinate was also accomplished, whereas esterification with benzoate and pivaloate was unsuccessful.
