CAS 1808-63-5
:(3β)-3-Hydroxy-16-methylpregna-5,16-dien-20-one
Description:
(3β)-3-Hydroxy-16-methylpregna-5,16-dien-20-one, commonly known as a synthetic steroid, is characterized by its structural features that include a steroid backbone with specific functional groups. This compound has a hydroxyl group at the 3β position and a methyl group at the 16 position, contributing to its biological activity. It is a derivative of progesterone and exhibits properties that can influence various physiological processes, including hormonal regulation. The presence of the double bonds in the steroid structure enhances its reactivity and interaction with biological receptors. This compound is often studied for its potential applications in medicine, particularly in hormone replacement therapies and contraceptive formulations. Its CAS number, 1808-63-5, is a unique identifier that facilitates the tracking and study of this substance in scientific literature and regulatory contexts. Overall, (3β)-3-Hydroxy-16-methylpregna-5,16-dien-20-one is significant in the field of pharmacology and biochemistry due to its steroidal nature and potential therapeutic uses.
Formula:C22H32O2
InChI:InChI=1S/C22H32O2/c1-13-11-19-17-6-5-15-12-16(24)7-9-21(15,3)18(17)8-10-22(19,4)20(13)14(2)23/h5,16-19,24H,6-12H2,1-4H3/t16-,17+,18-,19-,21-,22-/m0/s1
InChI key:InChIKey=WYOKDIKHIXWWOC-LXIBVNSESA-N
SMILES:C[C@@]12[C@]([C@]3([C@@]([C@]4(C)C(=CC3)C[C@@H](O)CC4)(CC1)[H])[H])(CC(C)=C2C(C)=O)[H]
Synonyms:- (3Beta)-3-Hydroxy-16-Methylpregna-5,16-Dien-20-One
- (3β)-3-Hydroxy-16-methylpregna-5,16-dien-20-one
- 3beta-Hydroxy-16-methylpregna-5,16-dien-20-one
- Pregna-5,16-dien-20-one, 3-hydroxy-16-methyl-, (3β)-
- Pregna-5,16-dien-20-one, 3β-hydroxy-16-methyl-
- 3β-Hydroxy-16-methylpregna-5,16-dien-20-one
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Found 2 products.
16-Methyl-16-dehydropregnenolone
CAS:Controlled Product<p>16-Methyl-16-dehydropregnenolone is a steroid that is used as an intermediate in the synthesis of other steroids. It is synthesized by the oxidation of tetrahydropyran with an aldehyde, followed by the addition of chloride to give 16-methyl-16-dehydropregnenolone. The acetonedicarboxylate group of 16-methyl-16-dehydropregnenolone can be removed by treatment with tert-butyl or cyclopentanedione, which yields intermediates for elaboration into other biologically active compounds such as steroids.</p>Formula:C22H32O2Purity:Min. 95%Color and Shape:PowderMolecular weight:328.49 g/mol

