(+)-Valencene - ≥70% , CAS No.4630-07-3

CAS: 4630-07-3 Cat. No.: V332824 Formula: C₁₅H₂₄ Peso molecolare: 204.35 Numero EC: 225-047-6 PubChem CID: 9855795

GRADE & PURITY ≥70%

Synonyms

(3R,4aS,5R)-4a,5-Dimethyl-3-isopropenyl-1,2,3,4,4a,5,6,7-octahydronaphthalene | EINECS 225-047-6 | UNII-96H21P91IG | ent-7betaH-eremophila-10(1),11-diene | 2-CHLOROPYRIDINE-6-CARBONITRILE | Tox21_302397 | NCGC00256249-01 | 7-(N,N-diethyliminium chloride |

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Panoramica

Valencene is a sesquiterpene that is an aroma component of citrus fruit and citrus-derived odorants. Valencene is biosynthesized from FPP by the CVS enzyme. It is a precursor to nootkatone, the main contributor to the aroma and flavor of grapefruit.

product description： 

(+)-Valencene is a sesquiterpene, which contains decalin framework and two methyl-bearing stereocenters. It is an aroma component of citrus fruit.

application：

(+)-Valencene can be used as a precursor to prepare:(+)-Nootkatone (a sesquiterpene) by dark singlet oxygenation；Benzoyloxyvalencene by reacting with tert-butyl peroxy benzoate via Kharasch−Sosnovsky allylic oxidation method；(+)-Lineariifolianone, a natural product.

Specifications

Sinonimi

(3R,4aS,5R)-4a,5-Dimethyl-3-isopropenyl-1,2,3,4,4a,5,6,7-octahydronaphthalene | EINECS 225-047-6 | UNII-96H21P91IG | ent-7betaH-eremophila-10(1),11-diene | 2-CHLOROPYRIDINE-6-CARBONITRILE | Tox21_302397 | NCGC00256249-01 | 7-(N,N-diethyliminium chloride |

Specifiche e purezza

≥70%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Tipo di azione

INHIBITOR

Purezza

≥70%

Nomi e identificatori

• Pubchem Sid: 504764987
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764987
• Sorrisi canonici: CC1CCC=C2C1(CC(CC2)C(=C)C)C
• IUPAC Name: (3R,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene
• InChIKey: QEBNYNLSCGVZOH-NFAWXSAZSA-N
• INCHI: 1S/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h7,12-13H,1,5-6,8-10H2,2-4H3/t12-,13-,15+/m1/s1
• Isomeri SMILES: C[C@@H]1CCC=C2[C@]1(C[C@@H](CC2)C(=C)C)C
• PubChem CID: 9855795
• Peso molecolare: 204.35

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Prenol lipids
• Subclass: Sesquiterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
• Alternative Parents: Polycyclic hydrocarbons Branched unsaturated hydrocarbons Cyclic olefins Unsaturated aliphatic hydrocarbons
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Eremophilane sesquiterpenoid - Branched unsaturated hydrocarbon - Polycyclic hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aliphatic homopolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.
• External Descriptors: Bisabolanes

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

Obiettivi associati (umani)

TYR Tclin Tyrosinase (717 Activities)

Discover Target: TYR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TRPV1 Tclin Vanilloid receptor (8273 Activities)

Discover Target: TRPV1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

B16-F10 (4610 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
• Sensibilità: Light sensitive
• Indice di rifrazione: 1.504
• Rotazione specifica [α]: +100±25°, neat
• Punto di infiammabilità (°F): 212.0 °F
• Punto di infiammabilità (°C): 100 °C
• Punto di ebollizione (°C): 274° C (lit.)
• Peso molecolare: 204.350 g/mol
• XLogP3: 5.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 204.188 Da
• Monoisotopic Mass: 204.188 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 297.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• 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