| Identification | Back Directory | [Name]
HEXESTROL | [CAS]
5635-50-7 | [Synonyms]
Esestrolo
NSC 229419
HEXOESTROL
HEXOESTROLUM
DIHYDRODIETHYLSTILBESTROL
3,4-DI(P-HYDROXYPHENYL)HEXANE
4,4'-(3,4-Hexanediyl)bisphenol
3,4-BIS(4-HYDROXYPHENYL)HEXANE
3,4-BIS-(P-HYDROXYPHENYL)-HEXANE
4,4'-(1,2-DIETHYLETHYLENE)DIPHENOL
4,4'-(1,2-Diethylethylene)bisphenol
MESO-3,4-BIS[4-HYDROXYPHENYL]-HEXANE
Phenol, 4,4'-(1,2-diethyl-1,2-ethanediyl)bis- | [EINECS(EC#)]
227-082-2 | [Molecular Formula]
C18H22O2 | [MDL Number]
MFCD00068996 | [MOL File]
5635-50-7.mol | [Molecular Weight]
270.37 |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
45 | [Safety Statements ]
53-45 | [RIDADR ]
3249 | [WGK Germany ]
2
| [RTECS ]
SL0560850
| [HazardClass ]
6.1(b) | [PackingGroup ]
III |
| Hazard Information | Back Directory | [Uses]
Vitestrol can be used in methods related to bioactive agents that convert from anions to molecules | [Definition]
ChEBI: Hexestrol is a stilbenoid. | [Brand name]
Synoestrolum. | [World Health Organization (WHO)]
Hexestrol is a stilbene derivative. See WHO comment for
diethylstilbestrol.
(Reference: (WHODI) WHO Drug Information, 77.1, 16, 1977) | [Purification Methods]
Crystallise meso-Hexestero from *benzene or aqueous EtOH (m 185-188o). The meso-dibenzoyl derivative has m 236-237o. The 3RS,4RS(±)-racemate [5776-72-7] crystallises from pet ether, *C6H6/pet ether, Et2O/pet ether, or MeOH/H2O and has m 128-129o . The (±)-dibenzoyl derivative has m 123-124o . The 3R,4R(+)-isomer [26614-21-1] and 3S,4S(-)-isomer [26614-22-2] crystallise from Et2O/pet ether with m 80 -80.5o and have [] D (+) and (-) 17.7o (c 5, EtOH). Their dibenzoyl derivatives have m 116.5o .[Beilstein 6 III 5503, 6 IV 6761.] They have estrogenic activity where optically active forms are more potent and they have antineoplastic activity. [Aboul-Enein et al. Anal Profiles Drug Subst 11 347 1982, J Am Chem Soc 65 4911941.] |
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