1,4-CHRYSENEQUINONE

Base Information

• Chemical Name: 1,4-CHRYSENEQUINONE
• CAS No.: 100900-16-1
• Molecular Formula: C18H10O2
• Molecular Weight: 258.276
• Hs Code.: 2914399090
• Mol file: 100900-16-1.mol

Synonyms:1,4-Chrysenequinone;Chrysene-1,4-quinone;Chrysene-1,4-dione;

Chemical Property of 1,4-CHRYSENEQUINONE

Chemical Property:

• Vapor Pressure: 4.14E-10mmHg at 25°C
• Melting Point: 210-212 °C
• Refractive Index: 1.761
• Boiling Point: 499.5 °C at 760 mmHg
• Flash Point: 184.7 °C
• PSA: 34.14000
• Density: 1.353 g/cm³
• LogP: 3.92820
• Storage Temp.: Refrigerator, under inert atmosphere
• Solubility.: Chloroform (Slightly, Sonicated), Ethyl Acetate (Very Slightly, Sonicated), Meth

Purity/Quality:

98%,99%, ^*data from raw suppliers

1,4-Chrysenequinone ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 20/21/22
• Safety Statements: 36

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 1,4-Chrysenequinone, is a polycyclic aromatic quinone, that can act as an activator of aryl hydrocarbon receptor (AhR).

Technology Process of 1,4-CHRYSENEQUINONE

There total 3 articles about 1,4-CHRYSENEQUINONE 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: 80.0%

1-vinylnaphthalene (826-74-4,29793-40-6) + (+/-)-2-(p-tolylsulfinyl)-1,4-benzoquinone → benz-1,4-phenanthrenequinone (100900-16-1)

Guidance literature:

In dichloromethane; at 20 ℃; for 18h; under 9000720 Torr;

DOI:10.1016/S0040-4039(97)00505-4

Reference yield:

1-vinylnaphthalene (826-74-4,29793-40-6) + p-benzoquinone (106-51-4) → benz-1,4-phenanthrenequinone (100900-16-1)

Guidance literature:

With acetic acid; at 100 ℃;

DOI:10.1021/ja01177a035

Reference yield:

1-hydroxy-chrysene (63019-38-5) → benz-1,4-phenanthrenequinone (100900-16-1)

Guidance literature:

With potassium nitrososulfonate;

upstream raw materials:

1-hydroxy-chrysene

1-vinylnaphthalene

p-benzoquinone

Downstream raw materials:

chrysene

Refernces