biological source
synthetic
Quality Level
application(s)
flavors and fragrances
SMILES string
O=C1CCCCCCCC=CCCCCCCC1
InChI
1S/C17H30O/c18-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-17/h1-2H,3-16H2/b2-1-
InChI key
ZKVZSBSZTMPBQR-UPHRSURJSA-N
signalword
Warning
hcodes
Hazard Classifications
Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Interaction of civetone with rat liver microsomal cytochrome P-450 and steroidogenic enzymes.
Biochemical pharmacology, 37(11), 2291-2293 (1988-06-01)
Natural product communications, 7(7), 913-915 (2012-08-23)
The synthesis of (Z)-civetone (1) is described starting from oleic acid (5) via a series of reactions, intermolecular olefin self-metathesis, bromination/dehydrobromination into acetylene, semi-hydrogenation and intramolecular Dieckmann macrocyclization.
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