29304-60-7

Basic information

• Product Name: 7-methyl-4-phenyl-1,2-dihydronaphthalene
• Synonyms: 7-methyl-4-phenyl-1,2-dihydronaphthalene
• CAS NO: 29304-60-7
• Molecular Weight: 220.314
• Mol File: 29304-60-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 7-methyl-4-phenyl-1,2-dihydronaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 7-methyl-4-phenyl-1,2-dihydronaphthalene(29304-60-7)
• EPA Substance Registry System: 7-methyl-4-phenyl-1,2-dihydronaphthalene(29304-60-7)

Safety Data

• Hazardous Substances Data: 29304-60-7(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 51015-29-3 6-methyl-3,4-dihydronaphthalen-1(2H)-one 
• 6936-14-7 1,2-dihydro-4-(4-methylphenyl)naphthalene 
• 591-17-3 meta-bromotoluene 
• 100-58-3 phenylmagnesium bromide 
• 22156-45-2 4-(m-tolyl)butanoic acid 
• 1875-89-4 2-(3-methylphenyl)ethanol 
• 855658-72-9 (3-methyl-phenethyl)-malonic acid diethyl ester 
• 92848-10-7 (3-Methyl-phenaethyl)-malonsaeure 
• 101552-29-8 1-methyl-4-(1-phenylbuta-1,3-dienyl)benzene 
• 39199-36-5 1-(2-chloroethyl)-3-methylbenzene 

Downstream Products

• 29304-61-8 6-methyl-1-phenylnaphthalene 

Relevant articles and documents

Conversion of Carbonyl Compounds to Olefins via Enolate Intermediate

A general and efficient protocol to synthesize substituted olefins from carbonyl compounds via nickel catalyzed C—O activation of enolates was developed. Besides ketones, aldehydes were also suitable substrates for the presented catalytic system to produce di- or tri- substituted olefins. It is worth noting that this approach exhibited good tolerance to highly reactive tertiary alcohols, which could not survive in other reported routes for converting carbonyl compounds to olefins. This method also showed good regio- and stereo-selectivity for olefin products. Preliminary mechanistic studies indicated that the reaction was accomplished through nickel catalyzed C—O activation of enolates, thus offering helpful contribution to current enol chemistry.