Anodyne| Dienestrol | |
|---|---|
 |
| Esters [] | |
|---|---|
| Dienestrol acetate | |
|
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C18H18O2[1] |
|---|---|
| Molecular mass | 266.3 g/mol[1] |
| Appearance | MINUTE NEEDLES FROM DILUTE ALC[1] |
| Odor | Odorless[1] |
| Predicted LogP | 5.4[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] |
| Chirality | achiral[2] |
| Identifiers [] | |
|---|---|
| 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] |
| Dosing |
|---|
Dienestrol
Dienestrol (also known as Dienoestrol, Dehydrostilbestrol, Cycladiene, Dienol, Estraguard, Follidiene, Oestrodiene, Estroral, Restrol or Estragard)
Chemistry
Dienestrol is typically found in the form of its acetate ester.
Stereochemistry
Dienestrol is a achiral mixture