Anodyne

E2-TMA
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Conformer structure via JSmol
Physical properties
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356.5 g/mol [1]
[1]
Structural Identifiers
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C23H32O3 [1]
[(8R,9S,13S,14S,17S)-3-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] 2,2-dimethylpropanoate [1]
C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2OC(=O)C(C)(C)C)CCC4=C3C=CC(=C4)O [1]
InChI=1S/C23H32O3/c1-22(2,3)21(25)26-20-10-9-19-18-7-5-14-13-15(24)6-8-16(14)17(18)11-12-23(19,20)4/h6,8,13,17-20,24H,5,7,9-12H2,1-4H3/t17-,18-,19+,20+,23+/m1/s1 [1]
InChIKeySLOFBKMZOOTTDZ-WCZGSDDISA-N [1]

Estradiol pivalate

(Redirected from Estradiol pivalate)

Estradiol pivalate (also known as Estradiol 17-pivalate, Estradiol, 17-pivalate, Estradiol monopivalate, Pivalic acid, 3-hydroxyestra-1,3,5(10)-trien-17β-yl ester or Estra-1,3,5(10)-triene-3,17-diol (17β)-, 17-(2,2-dimethylpropanoate))

Chemistry

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Estradiol pivalate is a absolute mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 10522263, Estradiol pivalate. Accessed July 7, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/10522263

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Estradiol pivalate. UNII: I12U06L6S4. Global Substance Registration System. Accessed July 7, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/I12U06L6S4