L(-)-Carvone - ≥99% , CAS No.6485-40-1

CAS: 6485-40-1 Cat. No.: C117707 Formule: C₁₀H₁₄O Poids moléculaire: 150.22 Beilstein Registry Number: 2206714 Numéro CE: 229-352-5

QUALITÉ & PURETÉ ≥99%

Synonyms

(R)-CARVONE (CONSTITUENT OF MYRRH) | 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (R)- | AKOS006343214 | Q-103514 | DTXCID5021413 | DTXSID7041413 | EN300-298834 | L-Carvone, >=97%, FCC, FG | (5R)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one | 07V

Storage

Room temperature,Argon charged

Shipped In

Normal

Vue d’ensemble

(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.

(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.

Spécifications

Synonymes

(R)-CARVONE (CONSTITUENT OF MYRRH) | 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (R)- | AKOS006343214 | Q-103514 | DTXCID5021413 | DTXSID7041413 | EN300-298834 | L-Carvone, >=97%, FCC, FG | (5R)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one | 07V

Spécifications et pureté

≥99%

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

Normal

Type d'action

INHIBITOR

Pureté

≥99%

Noms et identifiants

Pubchem Sid

488189748

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488189748

Sourires canoniques

CC1=CCC(CC1=O)C(=C)C

IUPAC Name

(5R)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one

InChIKey

ULDHMXUKGWMISQ-SECBINFHSA-N

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

Isomères SMILES

CC1=CC[C@H](CC1=O)C(=C)C

WGK Allemagne

2

RTECS

OS8650000

Poids moléculaire

150.22

Beilstein

2206714

Reaxy-Rn

1364206

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1364206&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Menthane monoterpenoids
• Alternative Parents: Monocyclic monoterpenoids Cyclohexenones Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexenone - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
• External Descriptors: Menthane monoterpenoids

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Miscible with alcohol, ether, chloroform, propylene glycol and mineral oils. Immiscible with water and glycerol.
• Sensibilité: Light and air sensitive
• Indice de réfraction: 1.495-1.502
• Rotation spécifique [α]: -61.5 ° (neat)
• Point d'éclair (°F): 201.2 °F
• Point d'éclair (°C): 88°C
• Point d'ébullition (°C): 227-230°C
• Poids moléculaire: 150.220 g/mol
• XLogP3: 2.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 150.104 Da
• Monoisotopic Mass: 150.104 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 223.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1