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(3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]quinoline

Base Information
  • Chemical Name:(3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]quinoline
  • CAS No.:32353-38-1
  • Molecular Formula:C19H15N
  • Molecular Weight:257.335
  • Hs Code.:
  • NSC Number:239348
  • DSSTox Substance ID:DTXSID20428520
  • Mol file:32353-38-1.mol
(3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]quinoline

Synonyms:32353-38-1;(3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]quinoline;AO-840/42717831;NSC239348;DTXSID20428520;YTSWLKWYRVTRMW-VBKFSLOCSA-N;NSC-239348;3-benzylidene-2,3-dihydro-1H-cyclopenta[b]quinoline

Suppliers and Price of (3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]quinoline
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
Total 5 raw suppliers
Chemical Property of (3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]quinoline
Chemical Property:
  • Vapor Pressure:1.94E-07mmHg at 25°C 
  • Boiling Point:437.3°C at 760 mmHg 
  • Flash Point:193°C 
  • PSA:12.89000 
  • Density:1.204g/cm3 
  • LogP:4.72160 
  • XLogP3:4.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:257.120449483
  • Heavy Atom Count:20
  • Complexity:366
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CC(=CC2=CC=CC=C2)C3=NC4=CC=CC=C4C=C31
  • Isomeric SMILES:C1C/C(=C/C2=CC=CC=C2)/C3=NC4=CC=CC=C4C=C31
Technology Process of (3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]quinoline

There total 4 articles about (3Z)-3-benzylidene-1,2-dihydrocyclopenta[b]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 indium(III) chloride; In tetrahydrofuran; at 120 ℃; for 24h; Sealed tube;
DOI:10.1016/j.tet.2016.03.004
Guidance literature:
Multi-step reaction with 3 steps
1: iron; hydrogenchloride / ethanol; water / 0.67 h / 95 °C
2: potassium hydroxide / ethanol; water / 0.5 h / 95 °C
3: indium(III) chloride / tetrahydrofuran / 24 h / 120 °C / Sealed tube
With hydrogenchloride; indium(III) chloride; iron; potassium hydroxide; In tetrahydrofuran; ethanol; water;
DOI:10.1016/j.tet.2016.03.004
Guidance literature:
Multi-step reaction with 2 steps
1: potassium hydroxide / ethanol; water / 0.5 h / 95 °C
2: indium(III) chloride / tetrahydrofuran / 24 h / 120 °C / Sealed tube
With indium(III) chloride; potassium hydroxide; In tetrahydrofuran; ethanol; water;
DOI:10.1016/j.tet.2016.03.004
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