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Ethyl 5-nitrobenzofuran-2-carboxylate

Base Information Edit
  • Chemical Name:Ethyl 5-nitrobenzofuran-2-carboxylate
  • CAS No.:69604-00-8
  • Molecular Formula:C11H9NO5
  • Molecular Weight:235.196
  • Hs Code.:29329990
  • European Community (EC) Number:614-989-7,672-147-4
  • UNII:BWP4ZD8WZF
  • DSSTox Substance ID:DTXSID50989694
  • Wikidata:Q72476337
  • Mol file:69604-00-8.mol
Ethyl 5-nitrobenzofuran-2-carboxylate

Synonyms:Ethyl 5-nitrobenzofuran-2-carboxylate;69604-00-8;69404-00-8;ethyl 5-nitro-1-benzofuran-2-carboxylate;2-Benzofurancarboxylic acid, 5-nitro-, ethyl ester;Ethyl 5-nitrobenzo[b]furan-2-carboxylate;BWP4ZD8WZF;5-Nitrobenzofuran-2-carboxylic acid ethyl ester;5-NITROBENZO[B]FURAN-2-CARBOXYLIC ACID ETHYL ESTER;MFCD00275272;ethyl 5-nitrobenzo[d]furan-2-carboxylate;UNII-BWP4ZD8WZF;SCHEMBL2249264;DTXSID50989694;AMY21658;BCP08877;CS-M1104;GEO-01364;AKOS005071959;BB-0814;AC-26406;ethyl-5-nitro-1-benzofuran-2-carboxylate;SY024789;E0950;Ethyl 5-nitrobenzofuran-2-carboxylate, 97%;FT-0620704;FT-0680847;2-Benzofurancarboxylicacid,5-nitro-,ethyl ester;I11522;5-Nitro-benzofuran-2-carboxylic acid ethyl ester;A836478;A866800;J-521153;J-640084;J-800067;W-200484

Suppliers and Price of Ethyl 5-nitrobenzofuran-2-carboxylate
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
  • Usbiological
  • 5-Nitrobenzofuran-2-carboxylic acid ethyl ester
  • 5g
  • $ 433.00
  • Usbiological
  • 5-Nitrobenzofuran-2-carboxylic acid ethyl ester
  • 25g
  • $ 619.00
  • TRC
  • Ethyl 5-nitrobenzofuran-2-carboxylate
  • 5g
  • $ 140.00
  • TCI Chemical
  • Ethyl 5-Nitrobenzofuran-2-carboxylate >97.0%(GC)
  • 25g
  • $ 158.00
  • TCI Chemical
  • Ethyl 5-Nitrobenzofuran-2-carboxylate >97.0%(GC)
  • 5g
  • $ 32.00
  • SynQuest Laboratories
  • Ethyl 5-nitrobenzo[b]furan-2-carboxylate
  • 1 g
  • $ 16.00
  • Sigma-Aldrich
  • Ethyl 5-nitrobenzofuran-2-carboxylate 97%
  • 5g
  • $ 126.00
  • Frontier Specialty Chemicals
  • Ethyl 5-nitrobenzofuran-2-carboxylate 97%
  • 1g
  • $ 16.00
  • Crysdot
  • Ethyl 5-nitrobenzofuran-2-carboxylate 95+%
  • 100g
  • $ 444.00
  • ChemScene
  • Ethyl 5-nitrobenzofuran-2-carboxylate 99.94%
  • 100g
  • $ 239.00
Total 106 raw suppliers
Chemical Property of Ethyl 5-nitrobenzofuran-2-carboxylate Edit
Chemical Property:
  • Appearance/Colour:Light yellow to light brown powder 
  • Vapor Pressure:2.34E-05mmHg at 25°C 
  • Melting Point:150 °C 
  • Refractive Index:1.603 
  • Boiling Point:359.7 °C at 760 mmHg 
  • Flash Point:171.3 °C 
  • PSA:85.26000 
  • Density:1.362 g/cm3 
  • LogP:3.04090 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • Solubility.:slightly sol. in Acetone 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:3
  • Exact Mass:235.04807239
  • Heavy Atom Count:17
  • Complexity:314
Purity/Quality:

98% *data from raw suppliers

5-Nitrobenzofuran-2-carboxylic acid ethyl ester *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCOC(=O)C1=CC2=C(O1)C=CC(=C2)[N+](=O)[O-]
  • Uses Deriatives of benzofuran-2-carboxylic acid are known for exhibiting various pharmacological activities such as selective adenosine A2A receptor antagonists, anti-inflammatory agents and local anaesthe tics. Benzofuran-2-carboxylic acids bearing benzoyl nitrogen such as Ethyl 5-Nitrobenzofuran-2-carboxylate, are used as DNA-binding groups, where the these structural subunits mimic natural antitumor agents such as duocarmycin and netropsin.
Technology Process of Ethyl 5-nitrobenzofuran-2-carboxylate

There total 15 articles about Ethyl 5-nitrobenzofuran-2-carboxylate 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 potassium carbonate; In N,N-dimethyl-formamide; at 85 - 90 ℃; for 15h; Inert atmosphere;
Guidance literature:
ethanol; 3,4-dibromo-6-nitrochroman-2-one; for 1h; Reflux;
With triethylamine; for 8h; Reflux;
Guidance literature:
With triethylamine; In ethanol; for 8h; Solvent; Reflux;
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