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4-(4-nitrophenoxy)picolinic acid

Base Information Edit
  • Chemical Name:4-(4-nitrophenoxy)picolinic acid
  • CAS No.:1184827-15-3
  • Molecular Formula:C12H8N2O5
  • Molecular Weight:260.206
  • Hs Code.:
  • Mol file:1184827-15-3.mol
4-(4-nitrophenoxy)picolinic acid

Synonyms:

Suppliers and Price of 4-(4-nitrophenoxy)picolinic acid
Supply Marketing:Edit
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
  • 4-(4-Nitrophenoxy)pyridine-2-carboxylicAcid
  • 100mg
  • $ 285.00
  • Matrix Scientific
  • 4-(4-Nitrophenoxy)pyridine-2-carboxylic acid 95%
  • 2.500g
  • $ 1486.00
  • AK Scientific
  • 4-(4-Nitrophenoxy)pyridine-2-carboxylicacid
  • 250mg
  • $ 407.00
  • A1 Biochem Labs
  • 4-(4-Nitrophenoxy)pyridine-2-carboxylicacid 95%
  • 2.5 g
  • $ 900.00
Total 2 raw suppliers
Chemical Property of 4-(4-nitrophenoxy)picolinic acid Edit
Chemical Property:
  • Boiling Point:466.6±35.0 °C(Predicted) 
  • Density:1.464±0.06 g/cm3(Predicted) 
Purity/Quality:

99% *data from raw suppliers

4-(4-Nitrophenoxy)pyridine-2-carboxylicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 4-(4-nitrophenoxy)picolinic acid

There total 4 articles about 4-(4-nitrophenoxy)picolinic 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:
With ethanol; sodium hydroxide; at 20 ℃; for 1h;
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / dichloromethane / 0.33 h / Cooling with ice
1.2: 0.5 h / Cooling with ice
2.1: chlorobenzene / 4 h / 130 °C / UV-irradiation
3.1: ethanol; sodium hydroxide / 1 h / 20 °C
With ethanol; triethylamine; sodium hydroxide; In dichloromethane; chlorobenzene;
Guidance literature:
Multi-step reaction with 4 steps
1.1: thionyl chloride / 24 h / 85 °C
2.1: triethylamine / dichloromethane / 0.33 h / Cooling with ice
2.2: 0.5 h / Cooling with ice
3.1: chlorobenzene / 4 h / 130 °C / UV-irradiation
4.1: ethanol; sodium hydroxide / 1 h / 20 °C
With thionyl chloride; ethanol; triethylamine; sodium hydroxide; In dichloromethane; chlorobenzene;
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