124931

(R)-(−)-Carvone

98%

• Sinónimos: (−)-Carvone, (R)-5-Isopropenyl-2-methyl-2-cyclohexenone, p-Mentha-6,8-dien-2-one, Carvol
• Fórmula empírica (notación de Hill): C₁₀H₁₄O
• Número de CAS: 6485-40-1
• Peso molecular: 150.22
• Beilstein/REAXYS Number: 2206714
• EC Number: 229-352-5
• MDL number: MFCD00001578
• UNSPSC Code: 12352115
• PubChem Substance ID: 24847635
• NACRES: NA.22

Propiedades

• vapor density: 5.2 (vs air)
• vapor pressure: 0.4 mmHg ( 20 °C)
• assay: 98%
• form: liquid
• optical activity: [α]20/D −61°, neat
• refractive index: n20/D 1.497 (lit.)
• bp: 227-230 °C (lit.)
• density: 0.959 g/mL at 25 °C (lit.)
• SMILES string: CC(=C)[C@@H]1CC=C(C)C(=O)C1
• InChI: 1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m1/s1
• InChI key: ULDHMXUKGWMISQ-SECBINFHSA-N

Descripción

General description

(R)-(−)-Carvone is a monoterpenoid. Its ozonolysis in the gaseous phase has been proposed. Aldehydes (formaldehyde) and biradicals were obtained as the major products. It participates in the diastereoselective synthesis of homochiral octalones.

Application

(R)-(−)-Carvone may be employed as starting reagent for the synthesis of enantiopure (R)-(+)-3-methyl-6-isopropenyl-cyclohept-3-enone-1, a useful intermediate formed during the synthesis of terpenoids. It may be employed as starting reagent for the synthesis of differently protected (4S,6R,7R)-trihydroxy-1-octyne derivatives.

Chiral starting material.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H302,H317
• pcodes: P261 - P264 - P272 - P280 - P301 + P312 - P302 + P352
• Hazard Classifications: Acute Tox. 4 Oral - Skin Sens. 1
• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 1
• flash_point_f: 192.2 °F - closed cup
• flash_point_c: 89 °C - closed cup
• ppe: Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter