| Record Information |
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| Version | 1.0 |
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| Created at | 2020-03-19 00:37:38 UTC |
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| Updated at | 2020-11-18 16:35:10 UTC |
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| CannabisDB ID | CDB000451 |
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| Secondary Accession Numbers | Not Available |
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| Cannabis Compound Identification |
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| Common Name | Beta-Fenchol |
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| Description | Beta-Fenchol also known as Beta-fenchyl alcohol or Exo-fenchol, belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing 2 rings, which are fused to each other. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes is known to occur mainly through the methyl-eritritol-phosphate (MEP) pathway in the plastids. Geranyl diphosphate (GPP) is a key intermediate in the biosynthesis of cyclic monoterpenes. GPP undergoes several cyclization reactions to yield a diverse number of cyclic arrangements. Beta-Fenchol is an isomer of Fenchol. Fenchol is a colorless or white solid, that occurs widely in nature. Fenchol gives basil its characteristic scent and comprises 15.9% of the volatile oils of some species of Aster ( Ref:DOI ). |
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| Structure | |
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| Synonyms | | Value | Source |
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| (+)-b-Fenchyl alcohol | Generator | | (+)-Β-fenchyl alcohol | Generator | | Fenchol, (1S-exo)-isomer | MeSH | | Fenchol, (endo)-isomer | MeSH | | 1,3,3-Trimethyl-2-norbornanol | MeSH | | Fenchol, ((endo)-(+-))-isomer | MeSH | | Fenchol, ((exo)-(+-))-isomer | MeSH | | Fenchyl alcohol | MeSH | | endo-Fenchol | MeSH | | Fenchol, (1S-endo)-isomer | MeSH | | Fenchol, (exo)-isomer | MeSH | | Fenchol | MeSH | | Fenchol, (1R-endo)-isomer | MeSH | | b-Fenchol | Generator | | Β-fenchol | Generator |
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| Chemical Formula | C10H18O |
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| Average Molecular Weight | 154.25 |
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| Monoisotopic Molecular Weight | 154.1358 |
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| IUPAC Name | (1R,2S,4S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol |
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| Traditional Name | (1R,2S,4S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol |
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| CAS Registry Number | 22627-95-8 |
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| SMILES | CC1(C)[C@H]2CC[C@](C)(C2)[C@@H]1O |
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| InChI Identifier | InChI=1S/C10H18O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m0/s1 |
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| InChI Key | IAIHUHQCLTYTSF-QXFUBDJGSA-N |
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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. |
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| Kingdom | Organic compounds |
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| Super Class | Lipids and lipid-like molecules |
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| Class | Prenol lipids |
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| Sub Class | Monoterpenoids |
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| Direct Parent | Bicyclic monoterpenoids |
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| Alternative Parents | |
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| Substituents | - Fenchane monoterpenoid
- Bicyclic monoterpenoid
- Cyclic alcohol
- Secondary alcohol
- Organic oxygen compound
- Hydrocarbon derivative
- Organooxygen compound
- Alcohol
- Aliphatic homopolycyclic compound
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| Molecular Framework | Aliphatic homopolycyclic compounds |
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| External Descriptors | Not Available |
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| Ontology |
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Not Available | | Physical Properties |
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| State | Solid |
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| Experimental Properties | | Property | Value | Reference |
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| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | logP | Not Available | Not Available |
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| Predicted Properties | [] |
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