Anodyne| Hexestrol | |
|---|---|
 |
| Esters [] | |
|---|---|
| Hexestrol dipropionate | |
|
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C18H22O2[1] |
|---|---|
| Molecular mass | 270.4 g/mol[1] |
| Appearance | NEEDLES FROM BENZENE, THIN PLATES FROM DIL ALC[1] |
| Odor | ODORLESS[1] |
| Predicted LogP | 5.2[1] |
| Melting point | 185-188 °C[1] |
| Solubility | FREELY SOL IN ETHER; SOL IN ACETONE, ALCOHOL, METHANOL, DILUTE SOLN OF ALKALI HYDROXIDES, VEGETABLE OILS UPON SLIGHT WARMING; SLIGHTLY SOL IN BENZENE, CHLOROFORM; PRACTICALLY INSOL IN WATER, DIL MINERAL ACIDS[1] |
| Chirality | achiral[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | 4-[(3S,4R)-4-(4-hydroxyphenyl)hexan-3-yl]phenol[1] |
| SMILES | CC[C@H](C1=CC=C(C=C1)O)[C@@H](CC)C2=CC=C(C=C2)O[1] |
| InChI | InChI=1S/C18H22O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,17-20H,3-4H2,1-2H3/t17-,18+[1] |
| InChIKey | PBBGSZCBWVPOOL-HDICACEKSA-N[1] |
| Dosing |
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Hexestrol
Hexestrol (also known as meso-Hexestrol, Cycloestrol, Hexoestrol, Mesohexestrol, Hexanoestrol, Erythrohexestrol, Estra-Plex, Hexestrofen, Hormoestrol or Estrifar)
Chemistry
Hexestrol is typically found in the form of its dipropionate ester.
Stereochemistry
Hexestrol is a achiral mixture