87797-13-5

Basic information

• Product Name: 1,2,3,4-tetrahydro-7-methoxy-1-(4'-methoxyphenyl)naphthalene
• Synonyms: 1,2,3,4-tetrahydro-7-methoxy-1-(4'-methoxyphenyl)naphthalene
• CAS NO: 87797-13-5
• Molecular Weight: 268.356
• Mol File: 87797-13-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,2,3,4-tetrahydro-7-methoxy-1-(4'-methoxyphenyl)naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-tetrahydro-7-methoxy-1-(4'-methoxyphenyl)naphthalene(87797-13-5)
• EPA Substance Registry System: 1,2,3,4-tetrahydro-7-methoxy-1-(4'-methoxyphenyl)naphthalene(87797-13-5)

Safety Data

• Hazardous Substances Data: 87797-13-5(Hazardous Substances Data)

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 35191-43-6 1-(4-bromo-butyl)-4-methoxy-benzene 
• 52244-70-9 4-(4-methoxyphenyl)butan-1-ol 
• 935-50-2 4,4-dimethoxycyclohexa-2,5-dienone 
• 4521-28-2 4-(4-Methoxyphenyl)butyric acid 
• 637-69-4 4-Methoxystyrene 
• 98-83-9 isopropenylbenzene 
• 6836-19-7 7-Methoxy-1-tetralone 
• 851330-27-3 7-methoxy-1-(4-methoxyphenyl)naphthalene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 87797-18-0 1-[4-(4,4-Dimethoxy-cyclohexa-2,5-dienylidene)-butyl]-4-methoxy-benzene 
• 859331-05-8 6-methoxy-4-(4-methoxyphenyl)-1,2-dihydronaphthalene 
• 150-76-5 4-methoxy-phenol 
• 87797-15-7 4-(4-methoxyphenyl)butyl triphenylphosphonium bromide 

Downstream Products

• 851330-27-3 7-methoxy-1-(4-methoxyphenyl)naphthalene 

Relevant articles and documents

Visible-Light-Mediated [4+2] Cycloaddition of Styrenes: Synthesis of Tetralin Derivatives

We report a formal [4+2] cycloaddition reaction of styrenes under visible-light catalysis. Two styrene molecules with different electronic or steric properties were found to react with each other in good yield and excellent chemo- and regioselectivity. This reaction provides direct access to polysubstituted tetralin scaffolds from readily available styrenes. Sophisticated tricyclic and tetracyclic tetralin analogues were prepared in high yield and up to 20/1 diasteroselectivity from cyclic substrates.

Ring selectivity in the Na/EtOH reduction of 1-aryl-7-methoxynaphthalenes

Na/EtOH reduction of 1-aryl-7-methoxynaphthalenes occurred preferentially at the A-ring when no substituents were present at the ortho-positions of the aryl group (up to 100% selectivity), to afford 1-aryl-7-methoxy-1,2,3,4- tetrahydronaphthalenes. Ortho-

An approach to the biomimetic synthesis of aryltetralin lignans

The BF3 catalysed cyclisation of 3-arylpropyl substituted quinone-methide ketals affords a mild, biomimetic route to aryltetralins. 1H- and 13C-NMR spectra of the products are reported.