| Weight | 154.253 g/mol |
|---|---|
| Formula | C10H18O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Piperitol
11063-75-5, 16721-39-4, 16721-38-3, 491-04-3
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- Short and Stereoselective Total Synthesis of Furano Lignans (.+-.)-Dihydrosesamin, (.+-.)-Lariciresinol Dimethyl Ether, (.+-.)-Acuminatin Methyl Ether, (.+-.)-Sanshodiol Methyl Ether, (.+-.)-Lariciresinol, (.+-.)-Acuminatin, and (.+-.)-Lariciresinol Monomethyl Ether and Furofuran Lignans (.+-.)-Sesamin, (.+-.)-Eudesmin, (.+-.)-Piperitol Methyl Ether, (.+-.)-Pinoresinol, (.+-.)-Piperitol, and (.+-.)-Pinoresinol Monomethyl Ether by Radical Cyclization of Epoxides Using a Transition-Metal Radical Source. (Journal of Organic Chemistry, 2002)
- Lipase-catalyzed resolution of p-menthan-3-ols monoterpenes: preparation of the enantiomer-enriched forms of menthol, isopulegol, trans- and cis-piperitol, and cis-isopiperitenol (Tetrahedron-asymmetry, 2003)
- A General Approach to the Asymmetric Synthesis of Lignans: (-)-Methyl Piperitol, (-)-Sesamin, (-)-Aschantin, (+)-Yatein, (+)-Dihydroclusin, (+)-Burseran, and (-)-Isostegane (Synthesis, 2002)
- A new stereocontrolled synthesis of diequatorial furofuran lignans having two different aryl groups : a synthesis of methyl piperitol (Tetrahedron Letters, 1992)
- Piperitol from Paulownia tomentosa (Planta Medica, 1987)
- PHOTOINDUCED MOLECULAR TRANSFORMATIONS. CLVIII: A TOTAL SYNTHESIS OF ()-METHYL PIPERITOL : AN UNSYMMETRICALLY SUBSTITUTED 2,6-DIARYL-3,7-DIOXABICYCLO3 .3.0OCTANE LIGNAN (Journal of Organic Chemistry, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC(C(CC1)C(C)C)O
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InChIKeyHPOHAUWWDDPHRS-UHFFFAOYSA-N
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