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Benzyl 1(2H)-quinolinecarboxylate

Base Information
  • Chemical Name:Benzyl 1(2H)-quinolinecarboxylate
  • CAS No.:17718-19-3
  • Molecular Formula:C17H15NO2
  • Molecular Weight:0
  • Hs Code.:2933499090
  • DSSTox Substance ID:DTXSID70170264
  • Nikkaji Number:J48.210B
  • Wikidata:Q83040167
  • Mol file:17718-19-3.mol
Benzyl 1(2H)-quinolinecarboxylate

Synonyms:Benzyl 1(2H)-quinolinecarboxylate;17718-19-3;benzyl 2H-quinoline-1-carboxylate;1(2H)-Quinolinecarboxylic acid, benzyl ester;1(2H)-Quinolinecarboxylic acid benzyl ester;BRN 1290195;DTXSID70170264

Suppliers and Price of Benzyl 1(2H)-quinolinecarboxylate
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
  • American Custom Chemicals Corporation
  • BENZYL 1(2H)-QUINOLINECARBOXYLATE 95.00%
  • 5MG
  • $ 504.33
Total 3 raw suppliers
Chemical Property of Benzyl 1(2H)-quinolinecarboxylate
Chemical Property:
  • Vapor Pressure:5.38E-07mmHg at 25°C 
  • Boiling Point:411.9°C at 760 mmHg 
  • Flash Point:202.9°C 
  • PSA:29.54000 
  • Density:1.211g/cm3 
  • LogP:3.92160 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:265.110278721
  • Heavy Atom Count:20
  • Complexity:360
Purity/Quality:

99% *data from raw suppliers

BENZYL 1(2H)-QUINOLINECARBOXYLATE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C=CC2=CC=CC=C2N1C(=O)OCC3=CC=CC=C3
Technology Process of Benzyl 1(2H)-quinolinecarboxylate

There total 4 articles about Benzyl 1(2H)-quinolinecarboxylate 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 sodium tetrahydroborate; In methanol; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/acs.joc.7b02860
Guidance literature:
quinoline; With diisobutylaluminium hydride; In diethyl ether; at 0 ℃; for 2h;
benzyl haloformate; In diethyl ether; at 0 - 20 ℃;
DOI:10.1021/acs.orglett.9b01433
Guidance literature:
With sodium tetrahydroborate; In methanol; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/acs.orglett.0c00113
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