54367-97-4

Basic information

• Product Name: Cyclohexanone, 2-(2-naphthalenyl)-
• CAS NO: 54367-97-4
• Molecular Formula: C16H16O
• Molecular Weight: 224.302
• Mol File: 54367-97-4.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-(2-naphthalenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-(2-naphthalenyl)-(54367-97-4)
• EPA Substance Registry System: Cyclohexanone, 2-(2-naphthalenyl)-(54367-97-4)

Safety Data

• Hazardous Substances Data: 54367-97-4(Hazardous Substances Data)

Upstream product

• 21473-01-8 2-naphthalenylmagnesium bromide 
• 822-87-7 2-Chlorocyclohexanone 
• 90-11-9 1-Bromonaphthalene 
• 108-94-1 cyclohexanone 
• 838826-68-9 2-(2-oxo-5-hexenyl)naphthalene 
• 32316-92-0 naphthalene-2-boronic acid 
• 6651-36-1 1-(Trimethylsilyloxy)cyclohexene 
• 612-55-5 2-iodonaphthalene 
• 580-13-2 2-bromonaphthalene 
• 70080-13-6 2-naphthylacetaldehyde 
• 377776-09-5 2-naphthalen-2-yl-cyclohexanol 
• 54607-03-3 2-(cyclohex-1-en-1-yl)naphthalene 

Downstream Products

• 167476-36-0 2-naphthyl-1-(trimethylsilyloxy)cyclohex-1-ene 
• 1041469-73-1 C₂₁H₃₀OSi₂ 
• 1402080-92-5 7-(naphthalen-2-yl)oxepan-2-one 
• 132104-10-0 6-(naphthalen-2-yl)-6-oxohexanoic acid 
• 179601-92-4 (1S,2R)-(-)-2-(naphthalen-2-yl)-cyclohexanol 
• 179601-87-7 (1R,2S)-(-)-2-(naphthalen-2-yl)-cyclohexanol 

Relevant articles and documents

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Enantioselective Protonation of Silyl Enol Ethers Catalyzed by a Chiral Pentacarboxycyclopentadiene-Based Bronsted Acid

The enantioselective protonation of silyl enol ethers was realized in the presence of a pentacarboxycyclopenta-1,3-diene-based chiral Bronsted acid catalyst with water as an achiral proton source to give the corresponding α-aryl ketones in good yields and up to 75percent ee.

p-Toluenesulfonic acid catalysed fluorination of α-branched ketones for the construction of fluorinated quaternary carbon centres

A p-toluenesulfonic acid catalyzed fluorination of α-branched ketones for the construction of fluorinated quaternary carbon centers has been developed, featuring a broad substrate scope, environmentally benign reaction conditions, and operational simplicity.