(+)-Fenchol

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For Research Use Only | Not For Clinical Use
CATAP2217029
CAS2217-02-9
Structure
MDL NumberMFCD00003760
Molecular Weight154.25
InChI KeyIAIHUHQCLTYTSF-OYNCUSHFSA-N
REAXYS Number2038082
Descriptionanalytical standard
Assay≥99.0% (sum of enantiomers, GC)
BP201-202 °C (lit.)
Formneat; gas chromatography (GC): suitable
Gradeanalytical standard
MP43-46 °C
REAXYS Number2038082
Size1G

1Biosynthesis of Monoterpenes. Enantioselectivity in the Enzymatic Cyclization of Linalyl Pyrophosphate to (-)-Endo-Fenchol

D M Satterwhite, C J Wheeler, R Croteau

J Biol Chem. 1985 Nov 15;260(26):13901-8.

PMID: 4055764

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1Biosynthesis of Monoterpenes. Stereochemistry of the Enzymatic Cyclization of Geranyl Pyrophosphate to (-)-Endo-Fenchol

R Croteau, D M Satterwhite, C J Wheeler, N M Felton

J Biol Chem. 1988 Oct 25;263(30):15449-53.

PMID: 3170591

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1Identification of the Maze in the Conformational Landscape of Fenchol

E M Neeman, T R Huet

Phys Chem Chem Phys. 2018 Oct 3;20(38):24708-24715.

PMID: 30225485

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1Roles of Human CYP2A6 and Rat CYP2B1 in the Oxidation of (+)-fenchol by Liver Microsomes

M Miyazawa, K Gyoubu

Xenobiotica. 2007 Sep;37(9):943-53.

PMID: 17992728

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1Vibrational Signatures of Chirality Recognition Between α-Pinene and Alcohols for Theory Benchmarking

Robert Medel, Caroline Stelbrink, Martin A Suhm

Angew Chem Int Ed Engl. 2019 Jun 11;58(24):8177-8181.

PMID: 30985978

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