| Weight | 284.399 g/mol |
|---|---|
| Formula | C19H24O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Estrone 3-methyl ether (1091-94-7, 1624-62-0)
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- 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)
- 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)
- Reactivation of human placental 17 beta,20 alpha-hydroxysteroid dehydrogenase affinity alkylated by estrone 3-(bromoacetate): topographic studies with 16 alpha-(bromoacetoxy)estradiol 3-(methyl ether). (Biochemistry, 1985)
- Steroids XLI. preparation of 9, 11-tritiated estrone-3-methyl ether and following syntheses of 17-CH2X-derivatives of estradiol (Journal of Labelled Compounds and Radiopharmaceuticals, 1974)
- Chiral hydrogenation of estrone-3-methyl ether on modified Raney nickel catalysts. (Steroids, 1993)
- Effect of estrone- and estriol-3-methyl ether on progesterone in decidual development. (1962)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)OC
-
InChIKeyBCWWDWHFBMPLFQ-UHFFFAOYSA-N
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Estrone 3-methyl ether
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