| Identification | Back Directory | [Name]
Methyl 2-Hexyl-3-oxocyclopentanecarboxylate | [CAS]
37172-53-5 | [Synonyms]
DIHYDROJASMONATE
Einecs 253-379-1
DIHYDROISOJASMONAT
EXOVERT HIGH IMPACT
RUBARBUS HIGH IMPACT
TROPALONE HIGH IMPACT
DIHYDRO ISOJASMONATE(TM)
Methyldihydroisojasmonate
dihydroisojasmonate methyl ester
Methyl (2-amyl-3-oxocyclopentyl)acetate
2-N-Hexy-3-methoxycarbonylcyclopentanone
Methyl 2-hexyl-3-oxocyclopentancarboxylat
methyl 2-hexyl-3-oxocyclopentanecarboxylate
methyl 2-hexyl-3-oxocyclopentane-1-carboxylate
2-hexyl-3-oxo-cyclopentanecarboxylicacimethylester
Cyclopentanecarboxylicacid,2-hexyl-3-oxo-,methylester
2-HEXYL-3-OXO-CYCLOPENTANECARBOXYLIC ACID, METHYL ESTER | [EINECS(EC#)]
253-379-1 | [Molecular Formula]
C13H22O3 | [MDL Number]
MFCD00458917 | [MOL File]
37172-53-5.mol | [Molecular Weight]
226.31 |
| Hazard Information | Back Directory | [Chemical Properties]
Methyl 2-Hexyl-3-oxocyclopentanecarboxylate is a colorless liquid with a longlasting,
floral, jasmine-like odor that has only little of the fatty aspect characteristic
of many jasmine fragrances. The product has not been found in nature.
The title compound can be prepared by condensing an alkyl ??-bromocaprylate
with a trialkyl propane-1,1,3-tricarboxylate to give a substituted cyclopentanone.
Hydrolysis, decarboxylation, and esterification of the resulting monocarboxylic
acid with methanol yield the desired ester. Trialkyl propane-1,1,3-
tricarboxylates can be prepared by Michael addition of dialkyl malonates to alkyl
acrylates.
The compound is used in perfumery in floral compositions. | [Flammability and Explosibility]
Notclassified | [Trade name]
Dihydro isojasmonateTM (PFW). |
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