| Identification | Back Directory | [Name]
C09663 | [CAS]
473-16-5 | [Synonyms]
C09663
Atractylol
α-Eudesmol
alpha-eudesmol
(2R)-1,2,3,4,4a,5,6,8aβ-Octahydro-α,α,4aα,8-tetramethyl-2-naphthalenemethanol
(2R)-1,2,3,4,4a,5,6,8aβ-Octahydro-α,α,4aα,8-tetramethyl-2α-naphthalenemethanol
2-Naphthalenemethanol, 1,2,3,4,4a,5,6,8a-octahydro-α,α,4a,8-tetramethyl-, (2R,4aR,8aR)- | [Molecular Formula]
C15H26O | [MOL File]
473-16-5.mol | [Molecular Weight]
222.37 |
| Chemical Properties | Back Directory | [Melting point ]
81-82 °C | [Boiling point ]
301.1±11.0 °C(Predicted) | [density ]
0.959±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C Freezer, Under inert atmosphere | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly) | [form ]
Solid | [pka]
15.12±0.29(Predicted) | [color ]
White to Off-White | [LogP]
4.650 (est) | [EPA Substance Registry System]
2-Naphthalenemethanol, 1,2,3,4,4a,5,6,8a-octahydro-.alpha.,.alpha.,4a,8-tetramethyl-, (2R,4aR,8aR)- (473-16-5) |
| Hazard Information | Back Directory | [Uses]
α-Eudesmol is an isomer of β-Eudesmol (E938600), a sesquiterpenoid known to induce neurite outgrowth. β-Eudesmol exhibits antiangiogenic activity. | [Definition]
ChEBI: A eudesmane sesquiterpenoid in which the eudesmane skeleton carries a hydroxy substituent at C-11 and has a double bond between C-3 and C-4. |
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