Cas no 2244-16-8 ((S)-(+)-Carvone)
(S)-(+)-Carvone Chemical and Physical Properties
Names and Identifiers
-
- (S)-2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enone
- (S)-(+)-p-Mentha-6,8-dien-2-one
- (S)-(+)-Carvone
- (S)-(+)-5-Isopropenyl-2-methyl-2-cyclohexenone
- D-CARVONE
- S-(+)-Carvone
- (+)-Carvone
- 2-Methyl-5-(1-methylethenyl)-2-cyclohexene-1-one
- CARVONE, (+)-(AS)
- D-(+)-Carvone
- D(+)-Carvone
- (+)-Carvone,(S)-(+)-Carvone,(S)-5-Isopropenyl-2-methyl-2-cyclohexenone,p-Mentha-6,8-dien-2-one
- (+)-Carvone,(S)-5-Isopropenyl-2-methyl-2-cyclohexenone,p-Mentha-6,8-dien-2-one
- (5S)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one
- (S)-5-Isopropenyl-2-methyl-2-cyclohexeno
- Carvol
- D(+)-Carvone,synthetic
- p-Mentha-6,8-dien-2-one
- D-1-Methyl-4-isopropenyl-6-cyclohexen-2-one
- D-p-Mentha-6,8,(9)-dien-2-one
- (S)-Carvone
- (+)-(S)-Carvone
- Carvone, (+)-
- d-Carvone (natural)
- (+)-(4S)-carvone
- (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one
- 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (5S)-
- (S)-2-Methyl-5-(1-methylvinyl)cyclohex-2-en-1-one
- p-M
- D-?Carvone
- l-p-mentha-1(6),8-dien-2-one
- (S)-5-isopropenyl-2-methylcyclohex-2-en-1-one
- (-)-p-Mentha 6,8-diene 2-one
- (S)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one
- (5S)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one
- l-1-methyl-4-isopropenyl-6-cyclohexen-2-one
- (R)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one
- (R)-5-isopropenyl-2-methylcyclohex-2-en-1-one
- p-Mentha-1,8-dien-6-one
- (-)-p-mentha-6,8-dien-2-one
- Carvone
- l-carvone
- (R)-(-)-carvone
- (R)-carvone
- (-)-Carvone
- (4R)-Carvone
- (-)-(R)-carvone
- (+)-p-Mentha 6,8-diene 2-one
- levo-carvone
- (5R)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one
- (-)-(4R)-carvone
-
- MDL： MFCD00062997
- Inchi： 1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3
- InChI Key： ULDHMXUKGWMISQ-UHFFFAOYSA-N
- SMILES： CC(C1CC(=O)C(C)=CC1)=C
- BRN： 2042970
Computed Properties
- Exact Mass: 150.10400
- Monoisotopic Mass: 150.104465
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 1
- Complexity: 223
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 1
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 5
- XLogP3: 2.4
- Topological Polar Surface Area: 17.1
Experimental Properties
- Color/Form: Colorless to light yellow oil with aromas of parsley, dill seeds and black bread
- Density: 0.960?g/mL?at 20?°C(lit.)
- Melting Point: 88.9 oC
- Boiling Point: 228-230?°C(lit.)
- Flash Point: Degrees Fahrenheit:192.2°F
Degrees Celsius:89°C - Refractive Index: n20/D 1.499
- Solubility: 1300mg/l
- Water Partition Coefficient: <0.1 g/100 mL at 25 oC
- Stability/Shelf Life: Stable. Combustible. Incompatible with strong oxidizing agents, strong reducing agents.
- PSA: 17.07000
- LogP: 2.48790
- Solubility: Soluble in propylene glycol, vegetable oil and mineral oil, miscible in ethanol, insoluble in glycerol and water.
- Specific Rotation: 57 o (c=neat)
- FEMA: 2249
- Merck: 1874
- Optical Activity: [α]20/D +61±2°, neat
- Sensitiveness: Easy to absorb moisture, sensitive to light and air
(S)-(+)-Carvone Security Information
-
Symbol:
- Prompt：warning
- Signal Word：Warning
- Hazard Statement： H317
- Warning Statement： P280
- Hazardous Material transportation number：UN 2810
- WGK Germany：1
- Hazard Category Code： 22
- Safety Instruction： S24/25
- FLUKA BRAND F CODES：8-9-23
- RTECS：OS8670000
-
Hazardous Material Identification：
- Packing Group：II
- Hazard Level：6.1(a)
- Safety Term：6.1(a)
- Packing Group：II
- Risk Phrases：R22
- Storage Condition：?20°C
- HazardClass：6.1(a)
- PackingGroup：II
- TSCA：Yes
(S)-(+)-Carvone Customs Data
- HS CODE：29142900
- Customs Data：
China Customs Code:
2914299000Overview:
2914299000. Other cycloalkanones without other oxygen-containing groups\Cyclic enone or cyclic terpenone. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:5.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, Acetone declared packaging
Summary:
2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%
(S)-(+)-Carvone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 435759-5ML |
(S)-(+)-Carvone |
2244-16-8 | 5ml |
￥336.16 | 2023-12-06 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 435759-25ML |
(S)-(+)-Carvone |
2244-16-8 | 25ml |
￥1115.22 | 2023-12-06 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | W224928-SAMPLE-K |
(S)-(+)-Carvone |
2244-16-8 | ≥96%, FG | 587.6 | 2021-05-17 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | W224928-100G-K |
(S)-(+)-Carvone |
2244-16-8 | ≥96%, FG | 100G |
1029.64 | 2021-05-17 | |
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | W224928-1KG-K |
(S)-(+)-Carvone |
2244-16-8 | ≥96%, FG | 1KG |
2117.76 | 2021-05-17 | |
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | W224928-5KG-K |
(S)-(+)-Carvone |
2244-16-8 | ≥96%, FG | 5KG |
9280.42 | 2021-05-17 | |
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 22070-1ML |
(S)-(+)-Carvone |
2244-16-8 | 1ml |
￥539.93 | 2023-10-26 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 22070-25ML |
(S)-(+)-Carvone |
2244-16-8 | 25ml |
￥994.47 | 2023-10-26 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 22070-100ML |
(S)-(+)-Carvone |
2244-16-8 | 100ml |
￥3552.89 | 2023-10-26 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 79245-100MG |
(S)-(+)-Carvone |
2244-16-8 | 100mg |
￥1482.65 | 2023-10-22 |
(S)-(+)-Carvone Suppliers
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(S)-(+)-Carvone Related Literature
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Lu-Lu Zhang,Yan Chen,Zhi-Jian Li,Xiao Li,Gang Fan Food Funct. 2022 13 3110
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Yu Zhou,Peng Luo,Li-Jun Xu,Wei Xu,Ren-Wang Jiang Org. Chem. Front. 2023 10 1119
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Chao Liu,Yucheng Jin,Dongdong Qi,Xu Ding,Huimin Ren,Hailong Wang,Jianzhuang Jiang Chem. Sci. 2022 13 7014
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Paola Rizzo,Eugenia Lepera,Gaetano Guerra Chem. Commun. 2014 50 8185
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Francisco Santamarta,Miguel Vilas,Emilia Tojo,Yagamare Fall RSC Adv. 2016 6 31177
Related Categories
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Menthane monoterpenoids
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- Natural Products and Extracts Plant Extracts Plant based Rhanterium epapposum
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Additional information on (S)-(+)-Carvone
Recent Advances in the Study of (S)-(+)-Carvone (CAS: 2244-16-8) and Its Applications in Chemical Biology and Medicine
(S)-(+)-Carvone (CAS: 2244-16-8), a naturally occurring monoterpene ketone, has garnered significant attention in recent years due to its diverse biological activities and potential applications in chemical biology and medicine. This research brief synthesizes the latest findings on (S)-(+)-Carvone, focusing on its pharmacological properties, mechanisms of action, and emerging therapeutic uses. The compound's stereospecificity and unique chemical structure make it a promising candidate for drug development and other biomedical applications.
Recent studies have elucidated the molecular mechanisms underlying (S)-(+)-Carvone's biological effects. For instance, research published in the Journal of Natural Products (2023) demonstrated its potent anti-inflammatory and antioxidant properties, mediated through the inhibition of NF-κB and MAPK signaling pathways. Another study in Bioorganic & Medicinal Chemistry Letters (2024) highlighted its antimicrobial activity against drug-resistant bacterial strains, suggesting potential applications in combating antibiotic resistance. These findings underscore the compound's multifaceted therapeutic potential.
In the realm of chemical biology, (S)-(+)-Carvone has been explored as a chiral building block for the synthesis of complex molecules. A 2024 study in Organic Letters detailed its use in asymmetric catalysis, enabling the efficient production of enantiomerically pure compounds. Additionally, its role as a flavor and fragrance agent has been expanded upon, with new research in Flavour and Fragrance Journal (2023) investigating its sensory properties and stability in various formulations.
From a medicinal chemistry perspective, structural analogs of (S)-(+)-Carvone have been designed to enhance its bioavailability and target specificity. Computational modeling studies, such as those published in the Journal of Chemical Information and Modeling (2024), have provided insights into structure-activity relationships, guiding the development of novel derivatives with improved pharmacokinetic profiles. These advancements are paving the way for preclinical evaluations of (S)-(+)-Carvone-based therapeutics.
Looking ahead, the integration of (S)-(+)-Carvone into drug delivery systems represents a promising avenue for research. Recent work in the International Journal of Pharmaceutics (2024) explored its encapsulation in nanocarriers to improve solubility and controlled release. Furthermore, ongoing clinical trials are investigating its efficacy in pain management and neurological disorders, with preliminary results expected in late 2024. These developments highlight the compound's translational potential and its growing importance in the pharmaceutical industry.
In conclusion, (S)-(+)-Carvone (CAS: 2244-16-8) continues to emerge as a versatile molecule with broad applications in chemical biology and medicine. The latest research underscores its therapeutic potential, while also revealing new challenges in optimizing its pharmacological properties. As investigations progress, this compound is poised to make significant contributions to drug discovery and development, offering novel solutions to unmet medical needs.
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