29304-65-2

Basic information

• Product Name: 3-Methyl-1-phenylnaphthalene
• Synonyms: 3-Methyl-1-phenylnaphthalene
• CAS NO: 29304-65-2
• Molecular Formula: C₁₇H₁₄
• Molecular Weight: 218.29306
• Mol File: 29304-65-2.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Methyl-1-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Methyl-1-phenylnaphthalene(29304-65-2)
• EPA Substance Registry System: 3-Methyl-1-phenylnaphthalene(29304-65-2)

Safety Data

• Hazardous Substances Data: 29304-65-2(Hazardous Substances Data)

Upstream product

• 3469-06-5 benzocyclobutenone 
• 19164-64-8 1-methylenebenzocyclobutane 
• 119-61-9 benzophenone 
• 115-11-7 isobutene 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 103-79-7 1-phenyl-acetone 
• 341028-97-5 4-chloro-2-methyl-[1]naphthylamine 
• 132277-09-9 1-chloro-3-methylnaphthalene 
• 77862-49-8 4-Methylene-2,2-diphenyltetrahydrofuran 
• 75-31-0 isopropylamine 
• 308378-45-2 (2-ethynylphenyl)(phenyl)methanone 
• 91-57-6 2-Methylnaphthalene 
• 94-36-0 dibenzoyl peroxide 
• 29304-64-1 Methyl-2-(cyclohexenyl-1')-4-naphthalin 

Relevant articles and documents

Rhodium(i)-catalysed skeletal reorganisation of benzofused spiro[3.3]heptanes: Via consecutive carbon-carbon bond cleavage

Skeletal reorganisation of benzofused spiro[3.3]heptanes has been achieved using rhodium(i) catalysts. The reaction of benzofused 2-(2-pyridylmethylene)spiro[3.3]heptanes proceeds via sequential C-C bond oxidative addition and β-carbon elimination. On the

Cyclization of (2-alkenylphenyl)carbonyl compounds to polycyclic arenes catalyzed by copper(II) trifluoromethanesulfonate or trifluoromethanesulfuric acid

Various polycyclic arenes, such as naphthalenes, tetrahydroantharacenes, tetrahydrotetracenes, dihydropentacenes, and dihydropentaphenes are prepared from 2-alkenylphenyl ketones and aldehydes by the catalytic use of copper(II) trifluoromethanesulfonate (Cu(OTf)2) or trifluoromethanesulfuric acid (TfOH). Copyright

Gold-Catalyzed Electrophilic Addition to Arylalkynes. A Facile Method for the Regioselective Synthesis of Substituted Naphthalenes

An interesting gold-catalyzed electrophilic addition to arylalkyne to synthesize substituted naphthalenes has been presented. Different metal hexafluoroantimonates have also been found to effect the transformation. Counter anion and oxo- and alkynophilicities of catalytic gold species might play an important role in this annulation reaction.