41848-73-1

Basic information

• Product Name: Methanone, phenyl(1-phenylcyclopentyl)-
• CAS NO: 41848-73-1
• Molecular Formula: C18H18O
• Molecular Weight: 250.34
• Mol File: 41848-73-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanone, phenyl(1-phenylcyclopentyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, phenyl(1-phenylcyclopentyl)-(41848-73-1)
• EPA Substance Registry System: Methanone, phenyl(1-phenylcyclopentyl)-(41848-73-1)

Safety Data

• Hazardous Substances Data: 41848-73-1(Hazardous Substances Data)

Upstream product

• 5422-88-8 phenyl cyclopentyl ketone 
• 100-42-5 styrene 
• 100-52-7 benzaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 4479-29-2 Hydroxy-cyclopentyl-diphenyl-methan 
• 7714-72-9 6,6-diphenylfulvene 
• 3400-45-1 cyclopentanecarboxylic acid 
• 77-57-6 1-phenyl-1-cyclopentanecarbonitrile 
• 52217-42-2 (1-chloro-cyclopentyl)-phenyl ketone 

Downstream Products

• 102207-07-8 C₁₇H₂₃NO 
• 76277-98-0 N-(1-phenylcyclopentylcarbonyl)morpholine 
• 59358-70-2 1,1'-Diphenyl-1,1'-bicyclopentyl 
• 22612-62-0 2,2-diphenylcyclohexanone 

Relevant articles and documents

N-Heterocyclic Carbene-Catalyzed Radical Relay Enabling Vicinal Alkylacylation of Alkenes

The N-heterocyclic carbene-catalyzed radical relay enables the vicinal alkylacylation of styrenes, acrylates and acrylonitrile using aldehydes and tertiary alkyl carboxylic acid-derived redox-active esters. This protocol introduces tertiary alkyl groups and acyl groups to C-C double bonds with complete regioselectivity to produce functionalized ketone derivatives. The radical relay mechanism involves single electron transfer from the enolate form of a Breslow intermediate and radical addition of the resultant alkyl radical to the alkene followed by radical-radical coupling.

NBS-promoted rearrangement of 1,1-diarylmethylenecyclopentane

The 1-aroyl-1-aryl-2-bromocyclopentanes 3a, 3b, 3c and 3d (Ar = C 6H5, 2-FC6H4, 3-FC6H 4, 4-FC6H4) were prepared from N-bromosuccinimide (NBS)-promoted rearrangement o