3771-17-3

Basic information

• Product Name: 4-(1,2,3,4-tetrahydro-1-naphthalenyl)phenol
• Synonyms: 4-(1,2,3,4-tetrahydro-1-naphthalenyl)phenol
• CAS NO: 3771-17-3
• Molecular Weight: 224.302
• Mol File: 3771-17-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-(1,2,3,4-tetrahydro-1-naphthalenyl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1,2,3,4-tetrahydro-1-naphthalenyl)phenol(3771-17-3)
• EPA Substance Registry System: 4-(1,2,3,4-tetrahydro-1-naphthalenyl)phenol(3771-17-3)

Safety Data

• Hazardous Substances Data: 3771-17-3(Hazardous Substances Data)

Upstream product

• 19353-89-0 1-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene 
• 108-24-7 acetic anhydride 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 108-95-2 phenol 
• 127461-76-1 1-(4-hydroxyphenyl)-1-methoxy-4-phenylbutane 
• 127461-75-0 1-(4-hydroxyphenyl)-1-<<(methoxyethoxy)methyl>oxy>-4-phenylbutane 
• 529-33-9 1,2,3,4-Tetrahydro-1-naphthol 
• 106-41-2 4-bromo-phenol 
• 67963-68-2 t-butyldimethylsilyl-4-bromophenol 
• 18328-11-5 3-benzyl propionaldehyde 
• 132777-00-5 1-<4-<(tert-butyldimethylsilyl)oxy>phenyl>-3-phenyl-propan-1-ol 
• 132777-36-7 1-<4-<(tert-butyldimethylsilyl)oxy>phenyl>-4-phenyl-butan-1-ol 
• 132777-07-2 1-<4-<(tert-butyldimethylsilyl)oxy>phenyl>-1-<<(methoxyethoxy)methyl>oxy>-4-phenylbutane 
• 21855-80-1 4-(3,4-dihydronaphthalen-1-yl)phenyl methyl ether 

Downstream Products

• 3771-19-5 nafenopin 
• 190519-46-1 Methyl 2-[2-[4-(1-tetralinyl)phenoxymethyl]phenyl]-3-methoxypropenoate 
• 41161-13-1 2-Methyl-2-[4-(1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-propionitrile 

Relevant articles and documents

A simple one pot synthesis of 1-aryltetralins

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Metal-Free C-O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes

A catalytic, metal-free intramolecular rearrangement of benzyl phenyl ethers using nitrosonium salt as a catalyst is described. The optimized reaction conditions enabled a catalytic and metal-free Friedel-Crafts alkylation reaction with benzylic alcohols, producing water as the stoichiometric byproduct. A comprehensive scope (>50 examples) for both approaches and application in drug synthesis were demonstrated. Mechanistic studies suggest a Lewis acid-based mechanism for the metal-free Friedel-Crafts reaction.

Hydroxy substituted phenyltetralines: compounds with affinity for estrogen and androgen receptors

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