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ethyl 2-amino-3-nitro-benzoate

Base Information Edit
  • Chemical Name:ethyl 2-amino-3-nitro-benzoate
  • CAS No.:61063-11-4
  • Molecular Formula:C9H10 N2 O4
  • Molecular Weight:210.189
  • Hs Code.:2922499990
  • Mol file:61063-11-4.mol
ethyl 2-amino-3-nitro-benzoate

Synonyms:Anthranilicacid, 3-nitro-, ethyl ester (7CI); 2-Amino-3-nitrobenzoic acid ethyl ester;3-Nitroanthranilic acid ethyl ester; Ethyl 2-amino-3-nitrobenzoate; NSC 696044

Suppliers and Price of ethyl 2-amino-3-nitro-benzoate
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
  • 2-Amino-3-nitrobenzoicAcidEthylEster
  • 1g
  • $ 495.00
  • Alichem
  • Ethyl2-amino-3-nitrobenzoate
  • 500mg
  • $ 831.30
  • Alichem
  • Ethyl2-amino-3-nitrobenzoate
  • 250mg
  • $ 504.00
Total 21 raw suppliers
Chemical Property of ethyl 2-amino-3-nitro-benzoate Edit
Chemical Property:
  • Vapor Pressure:4.35E-05mmHg at 25°C 
  • Melting Point:108 °C 
  • Boiling Point:350.6°C at 760 mmHg 
  • PKA:-2.83±0.25(Predicted) 
  • Flash Point:165.8°C 
  • PSA:98.14000 
  • Density:1.33g/cm3 
  • LogP:2.45810 
Purity/Quality:

98%,99%, *data from raw suppliers

2-Amino-3-nitrobenzoicAcidEthylEster *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 2-Amino-3-nitrobenzoic Acid Ethyl Ester, is a building block used in synthesis of various compounds, such as Ethyl 4-[4-(4-Substituted Piperidin-1-yl)]benzylpyrrolo[1,2-a]quinoxalinecarboxylate derivatives having Antiproliferative effect on human leukemia cells.
Technology Process of ethyl 2-amino-3-nitro-benzoate

There total 13 articles about ethyl 2-amino-3-nitro-benzoate 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 acetyl chloride; In methanol; ethyl acetate; at 0 - 20 ℃; for 64h;
Guidance literature:
sulfuric acid; for 240h; Heating / reflux;
Guidance literature:
With thionyl chloride; at 20 ℃; for 15h;
DOI:10.1016/j.ejmech.2013.04.051
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