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Naphth[2,3-c]acridine-5,8,14(13H)-trione

Base Information Edit
  • Chemical Name:Naphth[2,3-c]acridine-5,8,14(13H)-trione
  • CAS No.:3569-01-5
  • Molecular Formula:C21H11 N O3
  • Molecular Weight:325.323
  • Hs Code.:2933990090
  • European Community (EC) Number:222-665-8
  • DSSTox Substance ID:DTXSID9063083
  • Nikkaji Number:J216.208C
  • Wikidata:Q81990466
  • Mol file:3569-01-5.mol
Naphth[2,3-c]acridine-5,8,14(13H)-trione

Synonyms:Naphth[2,3-c]acridine-5,8,14(13H)-trione;3569-01-5;13H-Naphtho[2,3-c]acridine-5,8,14-trione;Naphtho[2,3-c]acridine-5,8,14(13H)-trione;Naphth(2,3-c)acridine-5,8,14(13H)-trione;13H-NAPHTHO(2,3-C)ACRIDINE-5,8,14-TRIONE;SCHEMBL6825452;DTXSID9063083;EINECS 222-665-8;AKOS000592916;Naphtho[2,3-c]acridine-5,8,14(13H)-trione #

Suppliers and Price of Naphth[2,3-c]acridine-5,8,14(13H)-trione
Supply Marketing:Edit
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
Total 4 raw suppliers
Chemical Property of Naphth[2,3-c]acridine-5,8,14(13H)-trione Edit
Chemical Property:
  • Vapor Pressure:3.03E-14mmHg at 25°C 
  • Boiling Point:597.6°Cat760mmHg 
  • PKA:-5.88±0.20(Predicted) 
  • Flash Point:231.8°C 
  • PSA:67.00000 
  • Density:1.425g/cm3 
  • LogP:3.45670 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:325.07389321
  • Heavy Atom Count:25
  • Complexity:614
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C4=C(C=C3)C(=O)C5=CC=CC=C5N4
Technology Process of Naphth[2,3-c]acridine-5,8,14(13H)-trione

There total 26 articles about Naphth[2,3-c]acridine-5,8,14(13H)-trione 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:
Guidance literature:
With sulfuric acid; at 100 - 110 ℃;
Guidance literature:
With aluminium trichloride; benzene;
Guidance literature:
Multi-step reaction with 2 steps
1: 1) NaNO2/H2SO4; 2) NaN3 / 1) AcOH, 20-25 deg C, 15-20 min; 2) H2O, 10-15 min
2: nitrobenzene / 7 h / Heating
With sodium azide; sulfuric acid; sodium nitrite; In nitrobenzene;
DOI:10.1007/BF00512807
Refernces Edit
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