Anodyne

EPP
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Physical properties
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404.5 g/mol [1]
6.5 [1]
Structural Identifiers
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C27H32O3 [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] 3-phenylpropanoate [1]
C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2OC(=O)CCC4=CC=CC=C4)CCC5=C3C=CC(=C5)O [1]
InChI=1S/C27H32O3/c1-27-16-15-22-21-11-9-20(28)17-19(21)8-10-23(22)24(27)12-13-25(27)30-26(29)14-7-18-5-3-2-4-6-18/h2-6,9,11,17,22-25,28H,7-8,10,12-16H2,1H3/t22-,23-,24+,25+,27+/m1/s1 [1]
InChIKeyLQWSQQKTZLDGME-RYIFMDQWSA-N [1]

Estradiol phenylpropionate

(Redirected from Estradiol phenylpropionate)

Estradiol phenylpropionate (also known as Estradiol-17-phenylpropionate, Estradiol 17-hydrocinnamate, Estradiol, 17-hydrocinnamate, Hydrocinnamic acid, 17-ester with estradiol, Estra-1,3,5(10)-triene-3,17β-diol 17-benzenepropionate, Estra-1,3,5(10)-triene-3,17-diol (17β)-, 17-benzenepropanoate, Estra-1,3,5(10)-triene-3,17β-diol 17-(benzenepropionate) or Nci60_002142)

Chemistry

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Estradiol phenylpropionate is a absolute mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 68577, Estradiol phenylpropionate. Accessed July 7, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/68577

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Estradiol phenylpropionate. UNII: LS956OGN6U. Global Substance Registration System. Accessed July 7, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/LS956OGN6U