Dienestrol | |
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Esters [] | |
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Dienestrol acetate | |
Molecular structure via molpic based on CDK |
Physical properties [] | |
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Molecular mass | 266.3 g/mol [1] |
Appearance | MINUTE NEEDLES FROM DILUTE ALC [1] |
Odor | Odorless [1] |
Melting point | 233-234 [1] |
Solubility | FREELY SOL IN ALC, METHANOL, ETHER, ACETONE, PROPYLENE GLYCOL; SOL IN CHLOROFORM, AQ SOLN OF ALKALI HYDROXIDES; SOLUBLE IN VEGETABLE OILS AFTER WARMING, BUT CRYSTALLIZES OUT ON STANDING; PRACTICALLY INSOL IN WATER, DIL ACIDS . [1] |
Predicted LogP | 5.4 [1] |
Structural Identifiers [] | |
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Molecular formula | C18H18O2 [1] |
IUPAC name | 4-[(2E,4E)-4-(4-hydroxyphenyl)hexa-2,4-dien-3-yl]phenol [1] |
SMILES | C/C=C(/C(=C/C)/C1=CC=C(C=C1)O)\C2=CC=C(C=C2)O [1] |
InChI | InChI=1S/C18H18O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h3-12,19-20H,1-2H3/b17-3+,18-4+ [1] |
InChIKey | NFDFQCUYFHCNBW-SCGPFSFSSA-N [1] |
Dienestrol
Dienestrol (also known as Dienoestrol, Dehydrostilbestrol, Cycladiene, Dienol, Estraguard, Follidiene, Oestrodiene, Estroral, Restrol or Estragard)
Chemistry
Esters []
Dienestrol is typically found in the form of its ester.
Stereochemistry []
Dienestrol is a achiral mixture