3604-60-2 Usage
Synthetic steroid hormone
17A-PREGN-5-EN-20-YNE-3B,17-DIOL is a synthetic steroid hormone, which means it is a chemically modified version of naturally occurring hormones.
Compound in the family of pregnane steroids
It belongs to a group of hormones called pregnane steroids, which are derived from the hormone pregnenolone.
Androgen and anabolic steroid
It has the potential to enhance male characteristics and promote muscle growth.
Potent androgen receptor agonist
The chemical structure of 17A-PREGN-5-EN-20-YNE-3B,17-DIOL includes a 17-hydroxy group and a double bond between the 5th and 6th carbons, making it a potent androgen receptor agonist.
Controlled substance
It is a controlled substance, meaning its use is regulated and restricted.
Research use
It is typically used in research settings to study its effects on the body and its potential applications in medical treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 3604-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3604-60:
(6*3)+(5*6)+(4*0)+(3*4)+(2*6)+(1*0)=72
72 % 10 = 2
So 3604-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H30O2/c1-4-21(23)12-9-18-16-6-5-14-13-15(22)7-10-19(14,2)17(16)8-11-20(18,21)3/h1,5,15-18,22-23H,6-13H2,2-3H3
3604-60-2Relevant articles and documents
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Stavely
, p. 79 (1939)
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Sondheimer et al.
, p. 1742 (1956)
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METHODS FOR PREPARING 17-ALKYNYL-7-HYDROXY STEROIDS AND RELATED COMPOUNDS
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Page/Page column 13; 14, (2009/12/28)
The invention relates to processes for preparing 17-alkynyl-7-hydroxy- steroids, such as 17-Ethynyl-10R13S-dimethyl 2,3,4,7,8R,9S, 10,11,12,13,14S,15,16,17-hexadecahydro-1 H-cyclopenta[a]phenanthrene- 3R,7R,17S-triol (also referred to as 17α-ethynyl-androst-5-ene-3β,7β,17β-triol), that are essentially free of process impurities having binding activity at nuclear estrogen receptors.
Microbiological degradation of sterol side chains to a 17-keto group
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, (2008/06/13)
The side chains of sterols are degraded by fermentation with microorganisms capable of doing so in an improved manner by employing in such fermentations sterol derivatives of the formula STR1 wherein n is 1 or 2; R1 is H or lower alkyl, R2 is alkyl, whose chain optionally is interrupted by an oxygen atom, or when n is 2, also a hydrogen atom; and R3 is a sterol side chain.
