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4-Ethynyl-2-fluorobenzenamine

Base Information
  • Chemical Name:4-Ethynyl-2-fluorobenzenamine
  • CAS No.:1008112-39-7
  • Molecular Formula:C8H6FN
  • Molecular Weight:135.141
  • Hs Code.:
  • Mol file:1008112-39-7.mol
4-Ethynyl-2-fluorobenzenamine

Synonyms:4-ethynyl-2-fluoroaniline

Suppliers and Price of 4-Ethynyl-2-fluorobenzenamine
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
  • 4-AMINO-3-FLUOROPHENYLACETYLENE 95.00%
  • 5MG
  • $ 501.67
  • Activate Scientific
  • 4-Ethynyl-2-fluorobenzenamine 95%
  • 1 g
  • $ 312.00
  • Activate Scientific
  • 4-Ethynyl-2-fluorobenzenamine 95%
  • 5 g
  • $ 897.00
  • Acrotein
  • 4-Ethynyl-2-fluorobenzenamine 95%
  • 5g
  • $ 660.00
  • Acrotein
  • 4-Ethynyl-2-fluorobenzenamine 95%
  • 0.5g
  • $ 146.67
Total 8 raw suppliers
Chemical Property of 4-Ethynyl-2-fluorobenzenamine
Chemical Property:
  • Boiling Point:213.6±30.0 °C(Predicted) 
  • PKA:1.71±0.10(Predicted) 
  • Density:1.16±0.1 g/cm3(Predicted) 
Purity/Quality:

97% *data from raw suppliers

4-AMINO-3-FLUOROPHENYLACETYLENE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 4-Ethynyl-2-fluorobenzenamine

There total 2 articles about 4-Ethynyl-2-fluorobenzenamine 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 methanol; potassium carbonate; at 20 ℃; for 0.5h;
DOI:10.1021/acsmedchemlett.6b00057
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 21 h / 20 °C / Inert atmosphere
2: potassium carbonate; methanol / 0.5 h / 20 °C
With methanol; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; potassium carbonate; triethylamine; In tetrahydrofuran; 1: |Sonogashira Cross-Coupling;
DOI:10.1021/acsmedchemlett.6b00057
Guidance literature:
With copper(l) iodide; nickel(II) chloride hexahydrate; N,N,N,N,-tetramethylethylenediamine; In tetrahydrofuran; at 20 ℃; for 24h;
DOI:10.1021/acsmedchemlett.6b00057
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