| Identification | Back Directory | [Name]
6-KETOESTRADIOL | [CAS]
571-92-6 | [Synonyms]
Nsc 147966
6-Oxoestradiol
6-KETOESTRADIOL
Estradiol-6-one
oestradiol-6-one
6-Oxo-17β-estradiol
6-Keto 17β-Estradiol
BETA-ESTRADIOL-6-ONE
6-KETO-17-BETA-ESTRADIOL
Estradiol Related CoMpound C
1,3,5-Estratriene-3,17β-diol-6-one
1,3,5(10)-Estratrien-3,17β-diol-6-one
1,3,5-ESTRATRIENE-3,17BETA-DIOL-6-ONE
1,3,5[10]-ESTRATRIENE-3,17BETA-DIOL-6-ONE
1,3,5(10)-ESTRATRIEN-3,17-BETA-DIOL-6-ONE
3,17β-Dihydroxyestra-1,3,5(10)-trien-6-one
3,17β-Dihydroxy-1,3,5(10)-estratrien-6-one
3,17BETA-DIHYDROXY-1,3,5[10]-ESTRATRIEN-6-ONE
(17b)-3,17-Dihydroxyestra-1,3,5(10)-trien-6-one
(17β)-3,17-Dihydroxyestra-1,3,5(10)-trien-6-one
Estra-1,3,5(10)-trien-6-one, 3,17-dihydroxy-, (17beta)- (9ci)
Estradiol Related Compound C (15 mg) (1,3,5(10)-estratrien-3,17beta-diol-6-one)
1,3,5-Estratriene-3,17β-diol-6-one, 3,17β-Dihydroxy-1,3,5(10)-estratrien-6-one, 6-Ketoestradiol
β-Estradiol-6-one,1,3,5-Estratriene-3,17β-diol-6-one, 3,17β-Dihydroxy-1,3,5(10)-estratrien-6-one, 6-Ketoestradiol
(8R,9S,13S,14S,17S)-3,17-dihydroxy-13-Methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-6-one | [EINECS(EC#)]
206-141-6 | [Molecular Formula]
C18H22O3 | [MDL Number]
MFCD00056457 | [MOL File]
571-92-6.mol | [Molecular Weight]
286.37 |
| Chemical Properties | Back Directory | [Melting point ]
281-283 °C | [Boiling point ]
478.9±45.0 °C(Predicted) | [density ]
1.249±0.06 g/cm3(Predicted) | [storage temp. ]
Refrigerator | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
9.36±0.60(Predicted) | [color ]
White to Off-White | [BRN ]
3208779 | [InChIKey]
ZHTDDOWJIRXOMA-YVEZLPLXSA-N | [CAS DataBase Reference]
571-92-6 |
| Hazard Information | Back Directory | [Uses]
A metabolite of Estradiol (E888000). | [Purification Methods]
-Estradiol-6-one forms plates from EtOH. The 3,17-diacetate has m 173-175o after recrystallisation from aqueous EtOH. [Longwell & Wintersteiner J Biol Chem 133 219 1940.] The UV has max at 255 and 326nm in EtOH [Slaunwhite et al. J Biol Chem 191 627 1951]. [Beilstein 8 IV 2398.] |
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