Anodyne| EA | |
|---|---|
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 314.4 g/mol [1] |
| Predicted LogP | 2.8 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C20H26O3 [1] |
| IUPAC name | [(8R,9S,13S,14S,17S)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] acetate [1] |
| SMILES | CC(=O)OC1=CC2=C(C=C1)[C@H]3CC[C@]4([C@H]([C@@H]3CC2)CC[C@@H]4O)C [1] |
| InChI | InChI=1S/C20H26O3/c1-12(21)23-14-4-6-15-13(11-14)3-5-17-16(15)9-10-20(2)18(17)7-8-19(20)22/h4,6,11,16-19,22H,3,5,7-10H2,1-2H3/t16-,17-,18+,19+,20+/m1/s1 [1] |
| InChIKey | FHXBMXJMKMWVRG-SLHNCBLASA-N [1] |
Estradiol acetate
(Redirected from Estradiol acetate)
Estradiol acetate (also known as Femring, Femtrace, Estradiol 3-acetate, Estradiol-3-acetate, Menoring, 3-O-Acetylestradiol, Estradiol, 3-acetate, β-Estradiol 3-acetate, 17β-Estradiol 3-acetate or E 3A)
Chemistry
Stereochemistry []
Estradiol acetate is a absolute mixture
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 9818306, Estradiol acetate. Accessed July 7, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/9818306
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Estradiol acetate. UNII: 5R97F5H93P. Global Substance Registration System. Accessed July 7, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/5R97F5H93P