23665-63-6

Basic information

• Product Name: beta-CYPERONE
• Synonyms: 2(3H)-Naphthalenone,4,4a,5,6-tetrahydro-1,4a-dimethyl-7-(1-methylethyl)-, (S)-; Eudesma-4,6-dien-3-one(7CI,8CI); (+)-b-Cyperone;b-Cyperone, (+)-
• CAS NO: 23665-63-6
• Molecular Formula: C₁₅H₂₂O
• Molecular Weight: 218.33458
• Product Categories: Miscellaneous Natural Products
• Mol File: 23665-63-6.mol

Chemical Properties

• Melting Point: 86 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 100-135 °C(Press: 0.1 Torr)
• Appearance: /
• Density: 0.98±0.1 g/cm3(Predicted)
• CAS DataBase Reference: beta-CYPERONE(CAS DataBase Reference)
• NIST Chemistry Reference: beta-CYPERONE(23665-63-6)
• EPA Substance Registry System: beta-CYPERONE(23665-63-6)

Safety Data

• Hazardous Substances Data: 23665-63-6(Hazardous Substances Data)

Upstream product

• 639-99-6 elemol 
• 51911-69-4 (1S,3S,6R)-3,7,7-Trimethyl-3-(3-oxo-pentyl)-bicyclo[4.1.0]heptan-2-one 
• 473-08-5 eudesma-4,11-dien-3-one 

Downstream Products

• 1837-16-7 eudesma-4,6-dien-3-one-(2,4-dinitro-phenylhydrazone) 
• 83093-44-1 Toluene-4-sulfonic acid 2-((2R,4aS)-4a,8-dimethyl-7-oxo-1,2,3,4,4a,5,6,7-octahydro-naphthalen-2-yl)-2-hydroxy-propyl ester 
• 473-10-9 carissone 

Relevant articles and documents

Reaction of elemol with acetic acid/perchloric acid: Characterization of a novel oxide and (+)-β-cyperone

The minor unidentified compounds of the acetic acid/perchloric acid dehydration of elemol (1) were fully characterized. The structure and relative configuration of the less polar fragrant compound 2, named elemoxide, was deduced by ID- and 2D-NMR data inc

Stereoselective total synthesis of (-)-α-eudesmol, a P/Q-type calcium channel blocker

Practical and stereoselective total synthesis of (-)-αeudesmol 1, a P/Q-type calcium channel blocker, has been achieved with the key step being a cyclopropane ring opening accompanying introduction of a hydroxyl group. (+)-Carissone is used as a key intermediate.