Chemistry:Testosterone formate
From HandWiki
Short description: Chemical compound
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| Other names | Testosterone carboxylate; Testosterone methanoate |
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| Formula | C20H28O3 |
| Molar mass | 316.441 g·mol−1 |
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Testosterone formate, also known as testosterone carboxylate or testosterone methanoate, as well as androst-4-en-17β-ol-3-one 17β-formate, is a synthetic, steroidal androgen and an androgen ester – specifically, the C17β formate ester of testosterone – which was first synthesized in the 1930s and was never marketed.[1][2][3][4]
See also
References
- ↑ Handbook of Aqueous Solubility Data, Second Edition. CRC Press. 19 April 2016. pp. 1233–. ISBN 978-1-4398-0246-5. https://books.google.com/books?id=cfFzJFthLCIC&pg=PA1233.
- ↑ Antitumor Steroids. Academic Press. 2 December 2012. pp. 76–. ISBN 978-0-323-13916-8. https://books.google.com/books?id=sxMBCIoDS1MC&pg=PA76.
- ↑ Elsevier's Encyclopaedia of Organic Chemistry: Series III: Carboisocyclic Condensed Compounds. Springer. 1 December 2013. pp. 3019–. ISBN 978-3-662-25863-7. https://books.google.com/books?id=HqHzCAAAQBAJ&pg=PA3019.
- ↑ "Recent Advances in the Field of Androgens". Cold Spring Harbor Symposia on Quantitative Biology 5: 34–43. 1937. doi:10.1101/SQB.1937.005.01.004. ISSN 0091-7451.
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