ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE

ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE
  • CAS No.:69604-00-8
Other grades of this product :
ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE Basic information
Product Name:ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE
Synonyms:ethyl 5-nitro-1-benzofuran-2-carboxylate;2-Benzofurancarboxylicacid, 5-nitro-, ethyl ester;5-Nitrobenzofuran-2-carboxylic acid ethyl esther;Vilazodone INT 1;Ethyl 5-nitrobenzofuran-2-carboxylate 97%;5-Nitrobenzofuran-2-carboxylic acid methyl ester;ETHYL 5-NITROBENZO[B]FURAN-2-CARBOXYLATE;ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE
CAS:69604-00-8
MF:C11H9NO5
MW:235.19
EINECS:
Product Categories:Benzofurans;Building Blocks;Esters;Fused Ring Systems;Chemical Synthesis;Heterocyclic Building Blocks
Mol File:69604-00-8.mol
ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE Chemical Properties
Melting point 152-156 °C
Boiling point 377.58°C (rough estimate)
density 1.362
refractive index 1.4950 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility slightly sol. in Acetone
form powder to crystal
color Light yellow to Amber to Dark green
Safety Information
Hazard Codes Xi
Safety Statements 22-24/25
WGK Germany 3
HazardClass IRRITANT
HS Code 29329990
MSDS Information
ProviderLanguage
ACROS English
ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE Usage And Synthesis
Chemical PropertiesLight yellow to light brown powder
UsesDeriatives 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.
UsesDeriatives of benzofuran-2-carboxylic acid are known for exhibiting various pharmacological activities such as selective adenosine A2A receptor antagonists, anti-inflammatory agents and local anaesthetics. 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.

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