1-Phenylnaphthalene

Base Information

• Chemical Name: 1-Phenylnaphthalene
• CAS No.: 605-02-7
• Molecular Formula: C16H12
• Molecular Weight: 204.271
• European Community (EC) Number: 210-081-6
• NSC Number: 5257
• UNII: 10NXC4G45Q
• DSSTox Substance ID: DTXSID8060539
• Nikkaji Number: J134.382C
• Wikidata: Q27251151
• Mol file: 605-02-7.mol

Synonyms:1-PHENYLNAPHTHALENE;605-02-7;Naphthalene, 1-phenyl-;1-Phenyl-naphthalene;C16H12;UNII-10NXC4G45Q;10NXC4G45Q;NSC 5257;NSC-5257;EINECS 210-081-6;PHENYLNAPHTHALENE;phenyl-napthalene;1-phenylnaphtalene;1-phenylnapthalene;p-(4-naphthyl)benzene;1-Phenylnaphthalene, 96%;DTXSID8060539;NSC5257;MFCD00003983;AKOS004901779;AC-18700;AS-57186;CS-0187929;FT-0608262;P0632;D82132;1-Phenylnaphthalene 10 microg/mL in Acetonitrile;A832755;10-Deacetylbaccatin III pound 10-DAB III pound(c);Q27251151

Chemical Property of 1-Phenylnaphthalene

Chemical Property:

• Appearance/Colour: clear colorless to yellow viscous liquid
• Vapor Pressure: 0.000219mmHg at 25°C
• Refractive Index: n20/D 1.664(lit.)
• Boiling Point: 336.4 °C at 760 mmHg
• Flash Point: 148.2 °C
• PSA: 0.00000
• Density: 1.081 g/cm³
• LogP: 4.50680
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 204.093900383
• Heavy Atom Count: 16
• Complexity: 214

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Safety Statements: S24/25:Avoid contact with skin and eyes.

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Other Classes -> Aromatic Hydrocarbons
• Canonical SMILES: C1=CC=C(C=C1)C2=CC=CC3=CC=CC=C32

Technology Process of 1-Phenylnaphthalene

There total 463 articles about 1-Phenylnaphthalene 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: 53.0%

1-phenyl-3,4-dihydronaphthalene (7469-40-1) → 1-phenylnaphthalene (605-02-7) + 1-phenyl-1,2,3,4-tetrahydronaphthalene (3018-20-0) + 1-phenyl-1,4-dihydronaphthalene (13387-49-0)

Guidance literature:

With propylamine; Irradiation;

Reference yield: 32.4%

1-bromovinylbenzene (98-81-7) → styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) + 2,5-Diphenyl-thiophene (1445-78-9) + 1-phenylnaphthalene (605-02-7) + α-styryl-β-styryl sulfide + phenylacetylene (536-74-3) + Benzo[b]thiophene (95-15-8,11095-43-5)

Guidance literature:

With hydrogen sulfide; at 150 ℃; for 7.5h; Product distribution; Heating; other time, other temperatures,;

Reference yield: 20.0%

1-bromovinylbenzene (98-81-7) → styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) + 2,5-Diphenyl-thiophene (1445-78-9) + 1-phenylnaphthalene (605-02-7) + α-styryl-β-styryl sulfide

Guidance literature:

With hydrogen sulfide; at 170 ℃; for 4h;

upstream raw materials:

pyrrolidine

diethyl ether

phenyllithium

1-Chloronaphthalene

Downstream raw materials:

2-phenylnaphthalene

fluoranthene

1-nitro-4-phenyl-naphthalene

1-bromo-4-phenylnaphthalene

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