Umbellulone , CAS No.546-78-1

CAS: 546-78-1 Cat. No.: U329539 Peso molecular: 150.22 Número EC: 806-143-2 PubChem CID: 442504

Synonyms

AC1L9CYT | DTXSID301016986 | Umbellulone | (1R,5S)-4-methyl-1-(propan-2-yl)bicyclo[3.1.0]hex-3-en-2-one | (1R,5S)-4-Methyl-1-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one | (1R,5S)-1-isopropyl-4-methyl-bicyclo[3.1.0]hex-3-en-2-one | MS-22850 | (-)-Umbellulone |

Storage

Store at -20°C,Desiccated

Shipped In

Ice chest + Ice pads

Descripción general

Umbellulone is a selective TRPA1 activator for proteomics research. Umbellulone is an offensive principle of the so-called "headache tree".

Specifications

Sinónimos

AC1L9CYT | DTXSID301016986 | Umbellulone | (1R, 5S)-4-methyl-1-(propan-2-yl)bicyclo[3.1.0]hex-3-en-2-one | (1R, 5S)-4-Methyl-1-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one | (1R, 5S)-1-isopropyl-4-methyl-bicyclo[3.1.0]hex-3-en-2-one | MS-22850 | (-)-Umbellulone |

Fuente

Umbellularia californica Nutt

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Desiccated

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

• Sonrisas canónicas: CC1=CC(=O)C2(C1C2)C(C)C
• IUPAC Name: (1R,5S)-4-methyl-1-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one
• InChIKey: LTTVJAQLCIHAFV-WCBMZHEXSA-N
• INCHI: 1S/C10H14O/c1-6(2)10-5-8(10)7(3)4-9(10)11/h4,6,8H,5H2,1-3H3/t8-,10+/m0/s1
• Isómeros SMILES: CC1=CC(=O)[C@@]2([C@H]1C2)C(C)C
• PubChem CID: 442504
• Peso molecular: 150.22

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Bicyclic monoterpenoids
• Alternative Parents: Cyclohexenones Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Bicyclic monoterpenoid - Thujane monoterpenoid - Cyclohexenone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
• External Descriptors: Cyclic monoterpenes

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

Propiedades químicas y físicas

• Índice de refracción: n20D1.53 (Predicted)
• Punto de ebullición (°C): ~214.1° C at 760 mmHg (Predicted)
• Peso molecular: 150.220 g/mol
• XLogP3: 1.600
• 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: 250.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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