2-Phenyl-1,2-dihydronaphthalene

Base Information

• Chemical Name: 2-Phenyl-1,2-dihydronaphthalene
• CAS No.: 62019-39-0
• Molecular Formula: C16H14
• Molecular Weight: 206.287
• DSSTox Substance ID: DTXSID80442080
• Mol file: 62019-39-0.mol

Synonyms:2-phenyl-1,2-dihydronaphthalene;Naphthalene, 1,2-dihydro-2-phenyl-;62019-39-0;DTXSID80442080;2-phenyl-1,2-dihydro-naphthalene

Chemical Property of 2-Phenyl-1,2-dihydronaphthalene

Chemical Property:

• XLogP3: 4.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 206.109550447
• Heavy Atom Count: 16
• Complexity: 247

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C=CC2=CC=CC=C21)C3=CC=CC=C3

Technology Process of 2-Phenyl-1,2-dihydronaphthalene

There total 13 articles about 2-Phenyl-1,2-dihydronaphthalene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

3-Phenyl-tetralol-1 (66858-77-3) → 2-phenyl-1,2-dihydronaphthalene (62019-39-0)

Guidance literature:

With oxalic acid; In water; for 6h; Heating;

Reference yield:

3-phenyl-1,2-dihydronaphthalene (20669-52-7) → 2-phenylnaphthalene (612-94-2) + 2-phenyl-1,2-dihydronaphthalene (62019-39-0)

Guidance literature:

at 900 ℃; under 0.1 Torr; Title compound not separated from byproducts; flash vacuum pyrolysis;

Reference yield:

(E)-1-styryl-2-vinylbenzene (58719-65-6) → 2-phenylnaphthalene (612-94-2) + 3-phenyl-1,2-dihydronaphthalene (20669-52-7) + 2-phenyl-1,2-dihydronaphthalene (62019-39-0)

Guidance literature:

at 900 ℃; Product distribution; Mechanism;

DOI:10.1021/jo00175a020

upstream raw materials:

2-Iodo-3-phenyl-1,2,3,4-tetrahydro-naphthalene

(E)-1-styryl-2-vinylbenzene

3-phenyl-1,2-dihydronaphthalene

3-Phenyl-tetralol-1

Downstream raw materials:

1,1-Dibrom-1a,2,3,7b-tetrahydro-exo-2-phenyl-1H-cyclopropanaphthalin

2-phenylnaphthalene

3-phenyl-1,2-dihydronaphthalene

3-phenyl-2-tetralone