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Floctafenic acid

Base Information
  • Chemical Name:Floctafenic acid
  • CAS No.:36783-34-3
  • Molecular Formula:C17H11F3N2O2
  • Molecular Weight:332.282
  • Hs Code.:2933499090
  • European Community (EC) Number:807-265-9
  • UNII:K9D19L5WTV
  • DSSTox Substance ID:DTXSID60190254
  • Nikkaji Number:J900.918C
  • Wikidata:Q27282128
  • Mol file:36783-34-3.mol
Floctafenic acid

Synonyms:floctafenic acid

Suppliers and Price of Floctafenic acid
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
  • TRC
  • FloctafenicAcid
  • 10mg
  • $ 150.00
  • Medical Isotopes, Inc.
  • FloctafenicAcid
  • 100 mg
  • $ 2200.00
  • AK Scientific
  • Floctafenicacid
  • 500mg
  • $ 2242.00
Total 4 raw suppliers
Chemical Property of Floctafenic acid
Chemical Property:
  • Vapor Pressure:2.67E-09mmHg at 25°C 
  • Boiling Point:461.1°Cat760mmHg 
  • Flash Point:232.7°C 
  • PSA:62.22000 
  • Density:1.451g/cm3 
  • LogP:4.76840 
  • Storage Temp.:Refrigerator 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:332.07726208
  • Heavy Atom Count:24
  • Complexity:458
Purity/Quality:

99% *data from raw suppliers

FloctafenicAcid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C(=C1)C(=O)O)NC2=C3C=CC=C(C3=NC=C2)C(F)(F)F
  • Uses Floctafenic Acid is an impurity of Floctafenine (F401700).
Technology Process of Floctafenic acid

There total 1 articles about Floctafenic acid 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:
Entspr. Me-Ester, Na2CO3;
Guidance literature:
Multi-step reaction with 2 steps
1: SOCl2; DMF / 2 h / Heating
2: Et3N / CH2Cl2 / 2 h / Heating
With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In dichloromethane;
DOI:10.1002/ardp.200400959
Guidance literature:
Multi-step reaction with 2 steps
1: SOCl2; DMF / 2 h / Heating
2: Et3N / CH2Cl2 / 2 h / Heating
With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In dichloromethane;
DOI:10.1002/ardp.200400959
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