| Weight | 284.399 g/mol |
|---|---|
| Formula | C19H24O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Estrone methyl ether (1091-94-7, 1624-62-0)
estrone 3-methyl ether, (+-)-isomer · estrone 3-methyl ether
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- Enantioselective ring construction: synthesis of (+)-estrone methyl ether (Journal of Organic Chemistry, 1987)
- Novel total syntheses of (+)-estrone 3-methyl ether, (+)-13.beta.-ethyl-3-methoxygona-1,3,5(10)-trien-17-one, and (+)-equilenin 3-methyl ether (Journal of Organic Chemistry, 1975)
- Total Synthesis of 19-Norsteroids. I. d,l-Estrone Methyl Ether (Journal of Organic Chemistry, 1963)
- The Formation of Five- and Six-membered Rings by the Acyloin Condensation. V. A Novel Conversion of 16-Ketoestradiol-3-methyl Ether to Estrone (Journal of the American Chemical Society, 1957)
- Boron annulation: total synthesis of ()-estrone methyl ether (Tetrahedron Letters, 1980)
- Steroid total synthesis. X. Optically active estrone precursors and racemic equilenin methyl ether (Journal of Organic Chemistry, 1973)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - estrone 3-methyl ether, (+-)-isomer
- estrone 3-methyl ether
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SMILESCC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)OC
-
InChIKeyBCWWDWHFBMPLFQ-UHFFFAOYSA-N
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Estrone methyl ether
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