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3,5-Difluoroquinoline

Base Information
  • Chemical Name:3,5-Difluoroquinoline
  • CAS No.:191861-15-1
  • Molecular Formula:C9H5F2N
  • Molecular Weight:165.142
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70172723
  • Nikkaji Number:J851.787H
  • Wikidata:Q83042805
3,5-Difluoroquinoline

Synonyms:3,5-Difluoroquinoline;191861-15-1;CCRIS 7838;DTXSID70172723

Suppliers and Price of 3,5-Difluoroquinoline
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 1 raw suppliers
Chemical Property of 3,5-Difluoroquinoline
Chemical Property:
  • Vapor Pressure:0.052mmHg at 25°C 
  • Boiling Point:242.7°Cat760mmHg 
  • Flash Point:100.6°C 
  • Density:1.319g/cm3 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:165.03900549
  • Heavy Atom Count:12
  • Complexity:163
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=C(C=C(C=N2)F)C(=C1)F
Technology Process of 3,5-Difluoroquinoline

There total 3 articles about 3,5-Difluoroquinoline 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:
5-amino-3-fluoroquinoline; With sodium nitrate; tetrafluoroboric acid; In water; at 0 ℃; for 1h;
In toluene; at 110 ℃; for 1h;
DOI:10.1021/jm1000908
Guidance literature:
Multi-step reaction with 3 steps
1.1: 38 percent / 61 percent HNO3; H2SO4 / 5 h / 20 °C
2.1: H2 / 5 percent Pd/C / benzene
3.1: isoamyl nitrite; 42 percent HBF4 / ethanol / 2 h / 0 °C
3.2: xylene / 3 h / Heating
With tetrafluoroboric acid; sulfuric acid; hydrogen; nitric acid; isopentyl nitrite; palladium on activated charcoal; In ethanol; benzene; 1.1: Nitration / 2.1: Reduction / 3.1: Schiemann reaction / 3.2: Deazotization;
DOI:10.1248/bpb.20.646
Guidance literature:
Multi-step reaction with 2 steps
1.1: H2 / 5 percent Pd/C / benzene
2.1: isoamyl nitrite; 42 percent HBF4 / ethanol / 2 h / 0 °C
2.2: xylene / 3 h / Heating
With tetrafluoroboric acid; hydrogen; isopentyl nitrite; palladium on activated charcoal; In ethanol; benzene; 1.1: Reduction / 2.1: Schiemann reaction / 2.2: Deazotization;
DOI:10.1248/bpb.20.646
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