2962-63-2

Basic information

• Product Name: cis-2-Amino-1-phenyl-1,2,3,4-tetrahydronaphthalene
• CAS NO: 2962-63-2
• Molecular Weight: 223.318
• Mol File: 2962-63-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: cis-2-Amino-1-phenyl-1,2,3,4-tetrahydronaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: cis-2-Amino-1-phenyl-1,2,3,4-tetrahydronaphthalene(2962-63-2)
• EPA Substance Registry System: cis-2-Amino-1-phenyl-1,2,3,4-tetrahydronaphthalene(2962-63-2)

Safety Data

• Hazardous Substances Data: 2962-63-2(Hazardous Substances Data)

Upstream product

• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 7469-40-1 1-phenyl-3,4-dihydronaphthalene 
• 101273-84-1 3-nitro-4-phenyl-1,2-dihydro-naphthalene 

Relevant articles and documents

1-Phenyl-3-amino-1,2,3,4-tetrahydronaphthalenes and Related Derivatives as Ligands for the Neuromodulatory ?3 Receptors: Further Structure-Activity Relationships

A series of 1-phenyl-3-amino-1,2,3,4-tetrahydronaphthalenes (1-phenyl-3-aminotetralins, PATs) previously was found to stimulate tyrosine hydroxylase activity and dopamine synthesis in rat brain through interaction with a novel ?3 receptor.Speci

Photoinduced Nucleophilic Addition of Ammonia and Alkylamines to Aryl-Substituted Alkenes in the Presence of p-Dicyanobenzene

The photoamination of 1,1-diphenylpropene (1a) with ammonia and some primary alkylamines in the presence of p-dicyanobenzene gave the corresponding N-substituted 2-amino-1,1-diphenylpropane (2a-e) along with the formation of 3-methyl-4,4-diphenylbutanenitrile (3a), 1,1-diphenylpropane (4a), 3,3-diphenylpropene (5), and diphenylmethane (6).In the case of 1,1-diphenylethene (1b), N-substituted 1-amino-2,2-diphenylethane (2f-h), 4,4-diphenylbutanenitrile (3b), and 1,1-diphenylethane (4b) were produced.In photoamination with t-butylamine in acetonitrile, 3a and 3b were mainly formed as a consequence of the incorporation of acetonitrile to 1a and 1b.The photoamination of 1-phenyl-3,4-dihydronaphthalene (1c) with isopropylamine or t-butylamine gave cis- and trans-N-substituted 1-phenyl-2-amino-1,2,3,4-tetrahydronaphthalenes (15 and 16) in a ratio of ca. 8:2.The mechanism of photoamination is discussed in terms of a photochemical electron transfer of 1 to p-dicyanobenzene followed by a nucleophilic addition of the amine to the cation radical of 1.