1,2-Phenanthrenequinone

Base Information

Chemical Name:1,2-Phenanthrenequinone
CAS No.:573-12-6
Molecular Formula:C14H8O2
Molecular Weight:208.2121
Hs Code.:
DSSTox Substance ID:DTXSID60205913
Nikkaji Number:J11.367K
Wikidata:Q83079649
Mol file:573-12-6.mol

Synonyms:1,2-phenanthrenedione;1,2-phenanthrenequinone

Suppliers and Price of 1,2-Phenanthrenequinone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
1,2-PHENANTHRAQUINONE 95.00%
5MG
$ 502.81

Total 6 raw suppliers

Chemical Property of 1,2-Phenanthrenequinone

Chemical Property:

Vapor Pressure:9.53E-07mmHg at 25°C
Melting Point:222 °C (decomp)
Boiling Point:404.3°Cat760mmHg
Flash Point:170.9°C
PSA：34.14000
Density:1.328g/cm³
LogP:2.61840
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:208.052429494
Heavy Atom Count:16
Complexity:356

Purity/Quality:

99% ^*data from raw suppliers

1,2-PHENANTHRAQUINONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC3=C2C=CC(=O)C3=O

Technology Process of 1,2-Phenanthrenequinone

There total 16 articles about 1,2-Phenanthrenequinone 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: 90.0%

: 605-55-0
phenanthren-2-ol

: 573-12-6
phenanthrene 1,2-quinone

Guidance literature:: With potassium peroxymonosulfate; sodium sulfate; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; Sodium 2-iodo-5-methylbenzenesulfonate; In ethyl acetate; at 40 ℃; for 2h; regioselective reaction;
DOI:10.3390/molecules17078604