42205-96-9

Basic information

• Product Name: (2-(4-methoxyphenyl)cyclopropyl)(phenyl)methanone
• Synonyms: (2-(4-methoxyphenyl)cyclopropyl)(phenyl)methanone
• CAS NO: 42205-96-9
• Molecular Weight: 252.313
• Mol File: 42205-96-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2-(4-methoxyphenyl)cyclopropyl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-(4-methoxyphenyl)cyclopropyl)(phenyl)methanone(42205-96-9)
• EPA Substance Registry System: (2-(4-methoxyphenyl)cyclopropyl)(phenyl)methanone(42205-96-9)

Safety Data

• Hazardous Substances Data: 42205-96-9(Hazardous Substances Data)

Upstream product

• 1774-47-6 trimethylsulfoxonium iodide 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 22252-15-9 trans-4-methoxychalcone 
• 70775-39-2 dimethylsulfoxonium methylide 

Downstream Products

• 1089672-16-1 3-(4-methoxyphenyl)-1,6-diphenylhexane-1,6-dione 
• 94540-81-5 2-(4-methoxyphenyl)-5-phenylfuran 
• 1234862-80-6 (3E)-4-(4-methoxyphenyl)-1-phenylbut-3-en-1-one 
• 153389-13-0 4-(4-methoxyphenyl)-1-phenyl-1-butanone 
• 258345-13-0 {3-[2-(4-methoxy-phenyl)-ethyl]-2-phenyl-1H-indol-5-yl}-acetic acid ethyl ester 
• 166115-93-1 4-(4-Methoxy-phenyl)-2-oxo-7-phenyl-4,5-dihydro-[1,3]oxazepine-3-sulfonyl chloride 
• 80775-75-3 4-<4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl>-4-(4-methoxyphenyl)-1-phenyl-1-butanone 
• 80775-82-2 4-<4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl>-4-(4-methoxyphenyl)-1-phenyl-1-butanone 
• 80775-76-4 4-(4-methoxyphenyl)-1-phenyl-4-(4-phenyl-1-piperazinyl)-1-butanone hydrochloride 

Relevant articles and documents

Visible-Light Induced Direct Synthesis of Polysubstituted Furans from Cyclopropyl Ketones

In this article, a photoredox protocol for the synthesis of furans via oxidative coupling of olefin generated in situ from cyclopropyl ketones with ketonic oxygen atom is presented. Moreover, bromination of furans in the presence of overstoichiometric oxidant has been achieved with high regioselectivity.

Further Investigations into the Mechanism of the Acid Catalysed Rearrangement of Aryl Substituted Cyclopropyl Ketones

The acid catalysed rearrangement of a number of aryl cyclopropyl ketones (2) to tetralones (3) were investigated in situ by 1H and 13C n.m.r. spectroscopy.The formation of oxycyclopentenyl intermediates (4) were observed.The involvement of a concurrent el