7270-99-7

Basic information

• Product Name: 1-Propanone, 2,2-dimethyl-1-(2-naphthalenyl)-
• CAS NO: 7270-99-7
• Molecular Formula: C15H16O
• Molecular Weight: 212.291
• Mol File: 7270-99-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 2,2-dimethyl-1-(2-naphthalenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 2,2-dimethyl-1-(2-naphthalenyl)-(7270-99-7)
• EPA Substance Registry System: 1-Propanone, 2,2-dimethyl-1-(2-naphthalenyl)-(7270-99-7)

Safety Data

• Hazardous Substances Data: 7270-99-7(Hazardous Substances Data)

Usage

Common uses

Production of fragrances and flavorings, manufacturing of pharmaceuticals and other chemical products

Physical properties

Volatile organic compound with a distinct odor

Industrial applications

Important ingredient in various industrial applications due to its chemical properties and uses

Upstream product

• 21473-01-8 2-naphthalenylmagnesium bromide 
• 3282-30-2 pivaloyl chloride 
• 630-18-2 tert-butyl isocyanide 

Downstream Products

• 126228-00-0 2,2-Dimethyl-1-(β-naphthyl)ethyl tosylate 

Relevant articles and documents

Electrochemical [4+2] Annulation-Rearrangement-Aromatization of Styrenes: Synthesis of Naphthalene Derivatives

We report the first electrochemical strategy to synthesize functionalized naphthalene derivatives through [4+2] annulation—rearrangement–aromatization from styrenes under mild conditions. The electrolysis does not require metals, oxidants and high valence substrates, indicating the atom and step-economy ideals. The dehydrodimer produced through [4+2] cycloaddition of 4-methoxy α-methyl styrene is isolated and proved to be the key intermediate for the following oxydehydrogenation to form carbon cation, which undergoes rearrangement–aromatization to afford the final products. This reaction represents a powerful access to construct multi-substituted naphthalene blocks in a single step.