37275

(+)-Dihydrocarvone

mixture of isomers

• Sinónimos: (2R,5R)-5-Isopropenyl-2-methylcyclohexanone
• Fórmula empírica (notación de Hill): C₁₀H₁₆O
• Número de CAS: 5524-05-0
• Peso molecular: 152.23
• Beilstein/REAXYS Number: 2044615
• EC Number: 226-872-4
• MDL number: MFCD00001636
• UNSPSC Code: 12352115
• PubChem Substance ID: 57649710
• NACRES: NA.22

Propiedades

• Quality Level: 100
• form: liquid
• optical activity: [α]20/D +20±2°, neat
• composition: n-(+)-dihydrocarvone, ~77% ; iso-(+)-dihydrocarvone, ~20%
• refractive index: n20/D 1.471
• density: 0.928 g/mL at 20 °C (lit.)
• SMILES string: CC1CCC(CC1=O)C(C)=C
• InChI: 1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h8-9H,1,4-6H2,2-3H3
• InChI key: AZOCECCLWFDTAP-UHFFFAOYSA-N

Descripción

General description

(+)-Dihydrocarvone, a monoterpenoid compound found in caraway oil, is a key building block to synthesize sesquiterpenes. It is generally produced either by the hydrogenation of carvone or oxidation of limonene.

Application

(+)-Dihydrocarvone may be used in the following processes:

• Synthesis of dispiro 1,2,4,5-tetraoxanes, which show potent anti-malarial activity.
• Synthesis of an epoxylactone by oxidation, which can undergo copolymerization with ε-caprolactone to form cross-linked copolymers with shape memory properties.
• Synthesis of α-Cyperone, a eudesmane type sesquiterpenoid compound with potent insecticidal activity.

Información de seguridad

• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 3
• flash_point_f: 215.6 °F - closed cup
• flash_point_c: 102 °C - closed cup
• ppe: Eyeshields, Gloves