Anodyne

Doisynoestrol
Doisynoestrol
Molecular structure via molpic based on CDK
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Physical properties
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298.4 g/mol [1]
4.6 [1]
Structural Identifiers
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C19H22O3 [1]
(1S,2R)-1-ethyl-7-methoxy-2-methyl-3,4-dihydro-1H-phenanthrene-2-carboxylic acid [1]
CC[C@H]1C2=C(CC[C@@]1(C)C(=O)O)C3=C(C=C2)C=C(C=C3)OC [1]
InChI=1S/C19H22O3/c1-4-17-16-7-5-12-11-13(22-3)6-8-14(12)15(16)9-10-19(17,2)18(20)21/h5-8,11,17H,4,9-10H2,1-3H3,(H,20,21)/t17-,19+/m0/s1 [1]
InChIKeyHZZSXUIUESWVSS-PKOBYXMFSA-N [1]

Doisynoestrol

Doisynoestrol (also known as Surestryl, Fenociclina, Fenocycline, Phenocyclin, Surestrine, 3-Methoxy-16,17-secoestra-1,3,5(10),6,8-pentaen-17-oic acid, dl-cis-Bisdehydrodoisynolic acid methyl ether, 2-Phenanthrenecarboxylic acid, 1-ethyl-1,2,3,4-tetrahydro-7-methoxy-2-methyl-, (1R,2S)-rel-, Dehydrofolliculinic acid or 7-Methylbisdehydrodoisynolic acid)

Chemistry

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(RS)-Doisynoestrol is a racemic mixture of the optical stereoisomers

See also []