2-Phenylphenanthrene

Base Information

• Chemical Name: 2-Phenylphenanthrene
• CAS No.: 4325-77-3
• Molecular Formula: C20H14
• Molecular Weight: 254.331
• Hs Code.: 2902909090
• European Community (EC) Number: 224-360-5
• DSSTox Substance ID: DTXSID20962979
• Nikkaji Number: J205.708E
• Wikidata: Q82944780
• Mol file: 4325-77-3.mol

Synonyms:2-Phenylphenanthrene;Phenanthrene, 2-phenyl-;4325-77-3;EINECS 224-360-5;2-Phenylphenanthren;2-Phenylphenanthrene #;DTXSID20962979;STK365507;AKOS005442880

Chemical Property of 2-Phenylphenanthrene

Chemical Property:

• Vapor Pressure: 1.19E-07mmHg at 25°C
• Boiling Point: 443.7°C at 760 mmHg
• Flash Point: 215.2°C
• PSA: 0.00000
• Density: 1.14g/cm³
• LogP: 5.66000
• XLogP3: 6.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 254.109550447
• Heavy Atom Count: 20
• Complexity: 314

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC3=C(C=C2)C4=CC=CC=C4C=C3

Technology Process of 2-Phenylphenanthrene

There total 26 articles about 2-Phenylphenanthrene 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: 84.0%

2-Vinyl-p-terphenyl (3365-06-8) → 2-phenylphenanthrene (4325-77-3)

Guidance literature:

With 4-tolyl iodide; boron trifluoride diethyl etherate; 3-chloro-benzenecarboperoxoic acid; In chlorobenzene; at 110 ℃; for 2h; chemoselective reaction;

DOI:10.1002/chem.201804786

Reference yield:

2-phenyl-3,4-dihydro-2H-phenanthren-1-one (857627-50-0) → 2-phenylphenanthrene (4325-77-3)

Guidance literature:

Multi-step reaction with 2 steps

1: Al(OiPr)3, acetone / propan-2-ol

2: Pd-C

With aluminum isopropoxide; acetone; palladium on activated charcoal; In isopropyl alcohol;

DOI:10.1021/jo01066a012

Reference yield:

2'-ethynyl-1,1':4',1''-terphenyl → 2-phenylphenanthrene (4325-77-3)

Guidance literature:

With silver trifluoromethanesulfonate; C₂₄H₂₇AuClO₃P; In toluene; at 70 ℃; for 16h;

DOI:10.1016/j.tetlet.2020.152333

upstream raw materials:

2-phenyl-3,4-dihydro-phenanthrene

2-cyclohexyl-phenanthrene

3,3-bis(methylthio)-1-phenyl-1-propan-1-one

(naphthalen-1-yl)methylmagnesium bromide

Downstream raw materials:

2-phenyl-9,10-phenanthrenequinone

2-phenyl-dibenzo[a,c]phenazine

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