5,6-Chrysenedione

Base Information

Chemical Name:5,6-Chrysenedione
CAS No.:2051-10-7
Molecular Formula:C18H10 O2
Molecular Weight:258.276
Hs Code.:2914399090
European Community (EC) Number:662-959-7
NSC Number:5192
UNII:3UZ6R8Y75B
DSSTox Substance ID:DTXSID10174509
Nikkaji Number:J7.309A
Wikidata:Q27258059
ChEMBL ID:CHEMBL1704614
Mol file:2051-10-7.mol

Synonyms:5,6-chrysenequinone

Suppliers and Price of 5,6-Chrysenedione

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
5,6-CHRYSENEQUINONE 98.00%
5MG
$ 502.44

TRC
5,?6-?Chrysenedione
250mg
$ 430.00

Total 7 raw suppliers

Chemical Property of 5,6-Chrysenedione

Chemical Property:

Vapor Pressure:1.59E-09mmHg at 25°C
Melting Point:239.5°C
Refractive Index:1.4800 (estimate)
Boiling Point:484°Cat760mmHg
Flash Point:210.3°C
PSA：34.14000
Density:1.336g/cm³
LogP:3.88580
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:258.068079557
Heavy Atom Count:20
Complexity:427

Purity/Quality:

99% ^*data from raw suppliers

5,6-CHRYSENEQUINONE 98.00% ^*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(=O)C(=O)C4=CC=CC=C34
Uses 5,?6-?Chrysenedione is a useful reactant for organic reactions. It is a polycyclic aromatic hydrocarbon quinones, and studied as possible carcinogens.

Technology Process of 5,6-Chrysenedione

There total 2 articles about 5,6-Chrysenedione 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: 63.0%

: 218-01-9
chrysene

: 132335-14-9
2-Phenylnaphthalene-1,2'-dicarboxaldehyde

: 2051-10-7
5,6-chrysenedione

Guidance literature:: With potassium bromate; In dichloromethane; water; acetonitrile; at 20 ℃; for 1h; Sonication;
DOI:10.1016/S1872-2067(15)61001-4

Reference yield:

: 218-01-9
chrysene

: 74087-85-7
3,3-dimethyldioxirane

: 15131-84-7,98243-92-6,98243-93-7
1a,11c-Dihydrochryseno<5,6-b>oxirene

: 2051-10-7
5,6-chrysenedione

: chrysene-5,6β:4b,10bα:11,12β-trioxide

Guidance literature:: In acetone; for 72h; Ambient temperature;
DOI:10.1016/S0040-4039(96)02006-0

Reference yield: 64.0%

: 2051-10-7
5,6-chrysenedione

: 4859-45-4
2-(2'-carboxyphenyl)-1-naphthoic acid

: 11-hydroxy-11H-benzo[a]fluorene-11-carboxylic acid

Guidance literature:: 5,6-chrysenedione; With 4,4'-dichlorobenzophenone; oxygen; sodium hydride; In tetrahydrofuran; mineral oil; at 0 - 20 ℃; for 0.5h; under 760.051 Torr;

With hydrogenchloride; In tetrahydrofuran; water; mineral oil; pH=1 - 2;
DOI:10.1016/j.tetlet.2012.10.127