precursor

Showing entry for Camphene

Identification

PhytoHub ID
PHUB000027
Name
Camphene
Synonyms
Not Available
CAS Number
Not Available
Average Mass
136.238
Monoisotopic Mass
136.125200515
Chemical Formula
C10H16
IUPAC Name
camphene
InChI Key
CRPUJAZIXJMDBK-UHFFFAOYSA-N
InChI Identifier
InChI=1S/C10H16/c1-7-8-4-5-9(6-8)10(7,2)3/h8-9H,1,4-6H2,2-3H3
SMILES
CC1(C)C2CCC(C2)C1=C
Structure
MOLSDF3D-SDFPDBSMILESInChI View 3D Structure

Calculated Properties

Solubility (ALOGPS)
6.21e-02 g/l
LogS (ALOGPS)
-3.34
LogP (ALOGPS)
4.56
Hydrogen Acceptors
0
Hydrogen Donors
0
Rotatable Bond Count
0
Polar Surface Area
0.0
Refractivity
43.6498
Polarizability
16.951480957680317
Formal Charge
0
Physiological Charge
0
pKa (strongest basic)
Not Available
pKa (strongest acidic)
Not Available
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Taxonomy

Family
Terpenoids
Class
Monoterpenoids
Sub-class
Not Available

Spectra

Record IDSourceDescriptionView
JP004717MassBankEI-B Spectrum - -, [M]+*View Spectra
JP006891MassBankEI-B Spectrum - -, [M]+*View Spectra
JP007538MassBankEI-B Spectrum - -, [M]+*View Spectra
JP011073MassBankEI-B Spectrum - -, [M]+*View Spectra
PS088402ReSpectN/A Spectrum - 20, [M+H]+View Spectra

Food Sources

NameGroup
RosemaryHerbs and Spices PublicationsShow

Metabolism

PrecursorMetaboliteSpeciesBiofluidsFormulaMonoisotopic mass
Camphene Camphene-2,10-glycolrabbiturineC10H18O2170.13067982 Publications
Camphene Camphene-10,2-glycolrabbiturineC10H18O2170.13067982 Publications
Camphene 6-exo-HydroxycamphenerabbiturineC10H16O152.120115135 Publications
Camphene 7-HydroxycamphenerabbiturineC10H16O152.120115135 Publications
Camphene 3-HydroxytricyclenerabbiturineC10H16O152.120115135 Publications
Camphene 10-hydroxytricyclenerabbiturineC10H16O152.120115135 Publications
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