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Indeno[1,2,3-de]quinoline

Base Information Edit
  • Chemical Name:Indeno[1,2,3-de]quinoline
  • CAS No.:206-55-3
  • Molecular Formula:C15H9N
  • Molecular Weight:203.2387
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID50174609
  • Nikkaji Number:J79.498H
  • Wikidata:Q83044703
  • Mol file:206-55-3.mol
Indeno[1,2,3-de]quinoline

Synonyms:indeno[1,2,3-de]quinoline;206-55-3;3-Azafluoranthene;INDENO(1,2,3-DE)QUINOLINE;SCHEMBL732391;DTXSID50174609

Suppliers and Price of Indeno[1,2,3-de]quinoline
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
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Total 0 raw suppliers
Chemical Property of Indeno[1,2,3-de]quinoline Edit
Chemical Property:
  • Vapor Pressure:8.4E-06mmHg at 25°C 
  • Melting Point:100-101 °C 
  • Boiling Point:385.5°Cat760mmHg 
  • PKA:4.97±0.30(Predicted) 
  • Flash Point:173°C 
  • PSA:12.89000 
  • Density:1.309g/cm3 
  • LogP:3.88220 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:203.073499291
  • Heavy Atom Count:16
  • Complexity:275
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C3=C4C2=CC=NC4=CC=C3
Technology Process of Indeno[1,2,3-de]quinoline

There total 7 articles about Indeno[1,2,3-de]quinoline 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 palladium diacetate; cesium pivalate; bis-diphenylphosphinomethane; In N,N-dimethyl-formamide; at 110 ℃; for 60h;
DOI:10.1021/jo048788h
Guidance literature:
Multi-step reaction with 4 steps
1: 63 percent / PPh3; DEAD / tetrahydrofuran / 4 h / 0 - 20 °C
2: 80 percent / ICl / CH2Cl2 / 1 h / -78 °C
3: 92 percent / NaOH; O2 / ethanol / 12 h / 50 °C / 760 Torr
4: 54 percent / 1,1-bis(diphenylphosphino)methane; CsO2CCMe3; Pd(OAc)2 / dimethylformamide / 60 h / 110 °C
With palladium diacetate; sodium hydroxide; oxygen; Iodine monochloride; triphenylphosphine; cesium pivalate; bis-diphenylphosphinomethane; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo048788h
Guidance literature:
Multi-step reaction with 4 steps
1: 63 percent / PPh3; DEAD / tetrahydrofuran / 4 h / 0 - 20 °C
2: 80 percent / ICl / CH2Cl2 / 1 h / -78 °C
3: 92 percent / NaOH; O2 / ethanol / 12 h / 50 °C / 760 Torr
4: 54 percent / 1,1-bis(diphenylphosphino)methane; CsO2CCMe3; Pd(OAc)2 / dimethylformamide / 60 h / 110 °C
With palladium diacetate; sodium hydroxide; oxygen; Iodine monochloride; triphenylphosphine; cesium pivalate; bis-diphenylphosphinomethane; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo048788h
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