76934-56-0

Basic information

• Product Name: (2-Benzo[1,3]dioxol-5-yl-cyclopropyl)-(3,4-dimethoxy-phenyl)-methanone
• Synonyms: (2-Benzo[1,3]dioxol-5-yl-cyclopropyl)-(3,4-dimethoxy-phenyl)-methanone
• CAS NO: 76934-56-0
• Molecular Weight: 326.349
• Mol File: 76934-56-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2-Benzo[1,3]dioxol-5-yl-cyclopropyl)-(3,4-dimethoxy-phenyl)-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Benzo[1,3]dioxol-5-yl-cyclopropyl)-(3,4-dimethoxy-phenyl)-methanone(76934-56-0)
• EPA Substance Registry System: (2-Benzo[1,3]dioxol-5-yl-cyclopropyl)-(3,4-dimethoxy-phenyl)-methanone(76934-56-0)

Safety Data

• Hazardous Substances Data: 76934-56-0(Hazardous Substances Data)

Upstream product

• 51116-22-4 (E)-1-(3,4-dimethoxyphenyl)-3-(3,4-methylenedioxyphenyl)-prop-2-en-1-one 
• 1774-47-6 trimethylsulfoxonium iodide 

Downstream Products

• 80816-89-3 6,7-dimethoxy-4-(3,4-methylenedioxyphenyl)-3,4-dihydronaphthalen-1(2H)-one 
• 76934-69-5 3,4-dimethoxyphenyl 3-hydroxy-3-(3,4-methylenedioxyphenyl)propyl ketone 

Relevant articles and documents

Reactions of Aryl Cyclopropyl Ketones. A New Synthesis of Aryl Tetralones

Aryl cyclopropyl ketones (2) cyclise to 1-tetralones (3) in the presence of a variety of acid catalysts under mild conditions.Open-chain carbinols (4) are also formed.The ratio of (3) to (4) is dependent on the aryl ring substituents.A cationic mechanism is proposed.Cyclopropyl ketones (1) do not react.Stereoelectronic factors involved in the reactivity of the rigig cyclopropyl ketone (12) are discussed.The reactions of selected phenolic cyclopropyl ketones have been investigated as anionic counterparts to the acid-catalysed reactions.No reaction is observed.