Isoborneol
Chemical compound / From Wikipedia, the free encyclopedia
Isoborneol is a bicyclic organic compound and a terpene derivative. The hydroxyl group in this compound is placed in an exo position. The endo diastereomer is called borneol. Being chiral, isoborneol exists as enantiomers.
Quick Facts Names, Identifiers ...
Names | |
---|---|
IUPAC name
(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-ol, (1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-ol | |
Identifiers | |
| |
3D model (JSmol) |
|
ChEBI |
|
ChEMBL | |
ChemSpider | |
PubChem CID |
|
UNII |
|
UN number | 1312 |
| |
| |
Properties | |
C10H18O | |
Molar mass | 154.253 g·mol−1 |
Appearance | white or colorless solid |
Melting point | 212–214 °C (414–417 °F; 485–487 K) + or -; 210–215 °C for rac |
Hazards | |
GHS labelling:[1] | |
Warning | |
H228 | |
P210, P240, P241, P280, P370+P378 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Close