51751-10-1

Basic information

• Product Name: 4-Phenyl-1,2,3,4-tetrahydro-1-naphthol
• Synonyms: 4-Phenyl-1,2,3,4-tetrahydro-1-naphthol
• CAS NO: 51751-10-1
• Molecular Weight: 224.302
• Mol File: 51751-10-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-Phenyl-1,2,3,4-tetrahydro-1-naphthol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Phenyl-1,2,3,4-tetrahydro-1-naphthol(51751-10-1)
• EPA Substance Registry System: 4-Phenyl-1,2,3,4-tetrahydro-1-naphthol(51751-10-1)

Safety Data

• Hazardous Substances Data: 51751-10-1(Hazardous Substances Data)

Upstream product

• 14578-67-7 4,4-diphenylbutanoic acid 
• 7498-88-6 4,4-diphenylbut-3-enoic acid 
• 16606-46-5 1-phenyl-1,2-dihydronaphtalene 
• 100-42-5 styrene 
• 1165952-91-9 cyclohexa-1,3-diene 

Downstream Products

• 7469-40-1 1-phenyl-3,4-dihydronaphthalene 
• 605-02-7 1-phenylnaphthalene 
• 83810-59-7 2-Oxo-4-phenyl-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid methyl ester 
• 83810-61-1 4-Phenyl-3,4-dihydro-naphthalene-1-carboxylic acid methyl ester 
• 150402-73-6 4-phenyl-2-tetralone 
• 16606-46-5 1-phenyl-1,2-dihydronaphtalene 

Relevant articles and documents

Efficient kinetic resolution in hydroboration of 1,2-dihydronaphthalenes

1-Substituted 1,2-dihydronaphthalenes undergo kinetic resolution during asymmetric hydroboration with Rh-QUINAP complexes.

Products of reaction between styrene and some radicals with 2,2-diphenyl-1-picrylhydrazyl

Addition of 2,2-diphenyl-1-picrylhydrazyl DPPH to styrene at 75 deg C results in little change in the amounts of cis- and trans-1,2-diphenylcyclobutane and 1,2,3,4-tetrahydro-1-phenylnaphthalene, in a slightly smaller amount of 1-phenylnaphthalene, and in a considerable increase in the amount of 1,2-dihydro-1-phenylnaphthalene that are formed.Formation of the styrene trimer 1,2,3,4-tetrahydro-1-phenyl-4-(1-phenylethyl)naphthalene is eliminated completely.Products derived from DPPH are 1-(4-nitrophenyl)-1-phenyl-2-picrylhydrazine 9 and 1--2,2-diphenylhydrazine, 10.DPPH intercepts the thermally formed Diels-Alder dimer of styrene as soon as it is formed to give the 1,2,3,4-tetrahydro-4-phenyl-1-naphthyl radical.Thermolysis of bis(1,2,3,4-tetrahydro-4-phenyl-1-naphthyl)diazene in the presence of DPPH yields 20percent of 10, 10percent of 1--2-(4-nitrophenyl)-2-phenylhydrazine and 9 while thermolysis of 1,2-bis(1-phenylethyl)diazene in the presence of DPPH yields 9 and 44percent of 1--2,2-diphenylhydrazine showing that substituted benzyl radicals efficiently displace the 4-nitro group of DPPH.The nitro group is transferred to an unsubstituted phenyl group of DPPH.