2,3-Fluoranthenedione

Base Information

• Chemical Name: 2,3-Fluoranthenedione
• CAS No.: 5386-28-7
• Molecular Formula: C16H8 O2
• Molecular Weight: 232.238
• Hs Code.: 2914399090
• DSSTox Substance ID: DTXSID80202121
• Nikkaji Number: J1.463.625K
• Wikidata: Q83075385
• Mol file: 5386-28-7.mol

Synonyms:F23Q cpd;fluoranthene-2,3-dione

Chemical Property of 2,3-Fluoranthenedione

Chemical Property:

• Vapor Pressure: 4.36E-08mmHg at 25°C
• Boiling Point: 444.2°C at 760 mmHg
• Flash Point: 190.6°C
• PSA: 34.14000
• Density: 1.41g/cm³
• LogP: 2.86410
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 232.052429494
• Heavy Atom Count: 18
• Complexity: 448

Purity/Quality:

97% ^*data from raw suppliers

2,3-FLUORANTHENEDIONE 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)C3=C4C2=CC(=O)C(=O)C4=CC=C3

Technology Process of 2,3-Fluoranthenedione

There total 2 articles about 2,3-Fluoranthenedione 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:

fluoranthene (206-44-0) → fluoranthene-2,3-quinone (5386-28-7) + 9-oxo-9H-fluorene-1-carboxylic acid (1573-92-8)

Guidance literature:

With chromium(VI) oxide; acetic acid;

DOI:10.1021/ja01171a502

Reference yield:

fluoranthene (206-44-0) → fluoranthene-2,3-quinone (5386-28-7) + 9-oxo-9H-fluorene-1-carboxylic acid (1573-92-8)

Guidance literature:

Reference yield:

fluoranthene-2,3-quinone (5386-28-7) → 3-phenylfluoranthen-2-ol

Guidance literature:

Multi-step reaction with 2 steps

1: 20 percent / p-toluenesulfonylhydrazide / methanol / 0.33 h / Heating

2: 38 percent / 3 h / Irradiation

With toluene-4-sulfonic acid hydrazide; In methanol;

DOI:10.1039/P29960002303

upstream raw materials:

fluoranthene

Downstream raw materials:

fluoreno[1,9-ab]phenazine

anti-2,3-dihydroxy-1,10b-epoxy-1,2,3,10b-tetrahydrofluoranthene