ChemicalBook--->CAS DataBase List--->545-46-0

545-46-0

545-46-0 Structure

545-46-0 Structure
IdentificationBack Directory
[Name]

UVAOL
[CAS]

545-46-0
[Synonyms]

UVAOL
UVAOL(SH)
UVAOL hplc
UVAOL WITH HPLC
12-URSEN-3B,28-DIOL
URS-12-ENE-3,28-DIOL
12-URSEN-3BETA, 28 DIOL
urs-12-ene-3beta,28-diol
3B,28-DIHYDROXY-URSA-12-EN
Uvaol,Urs-12-ene-3,28-diol
3BETA,28-DIHYDROXY-URSA-12-EN
(3S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol
[EINECS(EC#)]

208-888-3
[Molecular Formula]

C30H50O2
[MDL Number]

MFCD00009620
[MOL File]

545-46-0.mol
[Molecular Weight]

442.72
Chemical PropertiesBack Directory
[Melting point ]

223-225 °C(lit.)
[Boiling point ]

523.7±50.0 °C(Predicted)
[density ]

1.05±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly)
[form ]

Solid
[pka]

15.09±0.10(Predicted)
[color ]

White to Off-White
[LogP]

9.130 (est)
[CAS DataBase Reference]

545-46-0
Hazard InformationBack Directory
[Definition]

ChEBI: A natural product found in Rhododendron ferrugineum.
[Uses]

Uvaol can attenuate pleuritis and eosinophillic inflammation in mice that is induced by ovalbumin. It is an essential reagent in the synthesis of aminopropoxytriterpenoids that have anticancer activity.
Safety DataBack Directory
[Risk Statements ]

22
[Safety Statements ]

22-45
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

UVAOL(545-46-0)1HNMR
UVAOL(545-46-0)Raman
UVAOL(545-46-0)FT-IR
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