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| | HINESOL Basic information |
| Product Name: | HINESOL | | Synonyms: | 2-(6,10-Dimethylspiro[4.5]dec-6-en-2-yl)-2-propanol;HINESOL;HINESOL hplc;(2R,5S,10S)-α,α,6,10-Tetramethylspiro[4.5]dec-6-ene-2α-methanol;(2R,5S,10S)-alpha,alpha,6,10-Tetramethylspiro[4.5]dec-6-ene-2-methanol;Spiro(4.5)dec-6-ene-2-methanol, alpha,alpha,6,10-tetramethyl-, (2R-(2alpha,5alpha(S*)))-;2-[(2R,10S)-6,10-diMethylspiro[4.5]dec-6-en-2-yl]propan-2-ol;Spiro[4.5]dec-6-ene-2-methanol,a,a,6,10-tetramethyl-, (2R,5S,10S)- | | CAS: | 23811-08-7 | | MF: | C15H26O | | MW: | 222.37 | | EINECS: | | | Product Categories: | Miscellaneous Natural Products | | Mol File: | 23811-08-7.mol |  |
| | HINESOL Chemical Properties |
| Melting point | 59-60 °C | | Boiling point | 129 °C(Press: 4 Torr) | | density | 0.96 | | pka | 15.14±0.29(Predicted) | | Odor | at 100.00 %. spicy peppery woody | | Odor Type | spicy | | LogP | 4.703 (est) |
| | HINESOL Usage And Synthesis |
| Uses | Hinesol can be found in various essential oils that show antifugual activities (oils from agarwood of Aquilaria sinensis ), antimicrobial activities (oils from the Phebalium squamulosum species complex), anti-inflammatory activities ( oils from agarwood of Aquilaria agallocha) and anticancer activities (oil from Cedrelopsis grevei leaves). However, no reference shows that Hinesol is responsible for any of the above activities. | | Definition | ChEBI: Hinesol is a sesquiterpenoid. |
| | HINESOL Preparation Products And Raw materials |
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