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Thermo Scientific Chemicals
(S)-(+)-Carvone, 96%
CAS: 2244-16-8 | C10H14O | 150.221 g/mol
化学物質識別子
CAS2244-16-8
IUPAC Name(5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one
Molecular FormulaC10H14O
InChI KeyULDHMXUKGWMISQ-VIFPVBQESA-N
SMILESCC(=C)[C@H]1CC=C(C)C(=O)C1
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥95.0%
Optical Rotation58.0 ± 2.0? (neat)
Refractive Index1.4955-1.5030 @ 20?C
Appearance (Color)Clear colorless to white to yellow
FormLiquid
さらに表示
Carvones are used in the food and flavor industry. It is also used in air freshening products. Oils containing carvones are used in aromatherapy and alternative medicine. In organic synthesis, it is used as a starting material for the synthesis of terpenoid quassin natural product.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Carvones are used in the food and flavor industry. It is also used in air freshening products. Oils containing carvones are used in aromatherapy and alternative medicine. In organic synthesis, it is used as a starting material for the synthesis of terpenoid quassin natural product.
Solubility
Miscible with diethyl ether, ethanol and chloroform. Immiscible with water.
Notes
Incompatible with strong oxidizing agents and strong reducing agents. Keep the container tightly closed in a dry and well-ventilated place.
Carvones are used in the food and flavor industry. It is also used in air freshening products. Oils containing carvones are used in aromatherapy and alternative medicine. In organic synthesis, it is used as a starting material for the synthesis of terpenoid quassin natural product.
Solubility
Miscible with diethyl ether, ethanol and chloroform. Immiscible with water.
Notes
Incompatible with strong oxidizing agents and strong reducing agents. Keep the container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
General References:
- Senthil Kumaran, R.; Mehta, G. A versatile, RCM based approach to eudesmane and dihydroagarofuran sesquiterpenoids from (-)-carvone: a formal synthesis of (-)-isocelorbicol. Tetrahedron. 2015, 71 (19), 1718-1731.
- Huchelmann, A.; Gastaldo, C.; Veinante, M.; Zeng, Y.; Heintz, D.; Tritsch, D.; Schaller, H.; Rohmer, M.; Bach, T. J.; Hemmerlin, A. S-Carvone Suppresses Cellulase-Induced Capsidiol Production in Nicotiana tabacum by Interfering with Protein Isoprenylation. Plant Physiol. 2014, 164, 935-950.