53098-76-3

Basic information

• Product Name: (6E)-9-(3-Furyl)-2,6-dimethylnona-2,6-diene-4-one
• Synonyms: (6E)-9-(3-Furyl)-2,6-dimethylnona-2,6-diene-4-one;(6E)-9-(3-Furanyl)-2,6-dimethyl-2,6-nonadien-4-one
• CAS NO: 53098-76-3
• Molecular Formula: C15H20O2
• Molecular Weight: 232.32
• Mol File: 53098-76-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (6E)-9-(3-Furyl)-2,6-dimethylnona-2,6-diene-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: (6E)-9-(3-Furyl)-2,6-dimethylnona-2,6-diene-4-one(53098-76-3)
• EPA Substance Registry System: (6E)-9-(3-Furyl)-2,6-dimethylnona-2,6-diene-4-one(53098-76-3)

Safety Data

• Hazardous Substances Data: 53098-76-3(Hazardous Substances Data)

Upstream product

• 92631-20-4 Acetic acid (E)-8-furan-3-yl-1,1,5-trimethyl-2-phenylsulfanyl-8-(toluene-4-sulfonyl)-oct-5-enyl ester 
• 92631-24-8 Acetic acid (E)-6-furan-3-yl-3-methyl-1-(2-methyl-propenyl)-6-(toluene-4-sulfonyl)-hex-3-enyl ester 
• 92631-22-6 Acetic acid (2E,5E)-8-furan-3-yl-1,1,5-trimethyl-8-(toluene-4-sulfonyl)-octa-2,5-dienyl ester 
• 92631-25-9 6-hydroxy-1-p-tosyldendrolasin 
• 92631-11-3 1-(3-furyl)-4,8-dimethyl-1-p-tosylnona-3(E),7-diene 
• 92631-12-4 3-(tosylmethyl)furan 
• 6138-90-5 trans-geranyl bromide 
• 76890-83-0 (1'R,3'R,5'R)-1-(1'--5'-methyl-2',8'-dioxabicyclo<3,2,1>oct-3'-yl)-2-methylpropan-2-ol 
• 79421-75-3 (Z)-(S)-9-Furan-3-yl-2,6-dimethyl-nona-2,6-dien-4-ol 
• 76890-86-3 (4R,6R)-9-(furan-3'-yl)-2,6-dimethylnonane-2,4,6-triol 
• 76902-70-0 6-(furan-3-yl)-3-hydroxy-1-(2'-hydroxy-2'-methylprop-1'-yl)-3-methylhexyl acetate 
• 76890-87-4 Acetic acid (E)-(S)-6-furan-3-yl-3-methyl-1-(2-methyl-propenyl)-hex-3-enyl ester 
• 73204-33-8 eremoacetal 
• 870-63-3 prenyl bromide 

Downstream Products

• 36203-84-6 dihydrophymaspermone 

Relevant articles and documents

Facile Regio- and Stereo-specific Allylic Oxidation of gem-Dimethyl Olefins via Addition of Benzenesulphenyl Chloride. Synthesis of Allylic Oxygenated Terpenes

Novel and facile terminal trans-allylic and internal allylic oxidations of the gem-dimethyl olefin terminus of the terpenoids (1) are described which take place site-, regio-, and stereo-specificially via the same intermediate adduct between benzenesulphenyl chloride and (1).By this method, the allylic oxygenated terpenes (+/-)-nuciferal (11), (+/-)-ar-turmerone (12), (+/-)-ipsdienol (3c), neotorreyol (2e), (+/-)-6-hydroxydendrolasin (3e), and 6-oxodendrolasin (14) were synthesized.