17844-09-6

Basic information

• Product Name: 2-phenyl-6-methylheptan-4-one
• CAS NO: 17844-09-6
• Molecular Weight: 204.312
• Mol File: 17844-09-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-phenyl-6-methylheptan-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-6-methylheptan-4-one(17844-09-6)
• EPA Substance Registry System: 2-phenyl-6-methylheptan-4-one(17844-09-6)

Safety Data

• Hazardous Substances Data: 17844-09-6(Hazardous Substances Data)

Upstream product

• 2892-18-4 5-methyl-1-phenyl-hex-1-en-3-one 
• 74-88-4 methyl iodide 
• 78-77-3 Isobutyl bromide 
• 4593-90-2 3-phenylbutyric acid 
• 917-64-6 methyl magnesium iodide 

Downstream Products

• 17882-18-7 ar-juvabione 

Relevant articles and documents

SYNTHESIS OF JUVABIONE ANALOGUES

Alkylation of various β-ketoesters IIIa-d with bis(p-methoxycarbonylphenyl)bromomethane (II) and bis(p-chlorophenyl)bromomethane (VI) followed by cleavage of ethoxycarbonyl group or hydrolysis and esterification gave methoxycarbonylphenyl and chlorophenyl analogues of ar-juvabione, respectively.Condensation of bis(p-methoxycarbonylphenyl)methanol (IX) with isovaleryl and trichloroacetyl chloride gave isovalerate X and trichloroacetate XI, respectively, while the condensation of bis(p-chlorophenyl)methanol (XII) with isovaleryl chloride and citronellyl bromide yieldedisovalerate XIII and citronellyl ether XIV, respectively.The methoxycarbonylation of aryl-alkyl ketones XVa-d with oxalyl chloride and treatment with methanol furnished various ar-juvabione analogues XVIa-d.The compounds Vb, Vc, Vd, XVIb, and XVIc showed high activity against Dysdercus koenigii at 1μg concentration.