138173-83-8

Basic information

• Product Name: ethyl furo[2,3-c]pyridine-2-carboxylate
• Synonyms: ethyl furo[2,3-c]pyridine-2-carboxylate
• CAS NO: 138173-83-8
• Molecular Formula: C10H9NO3
• Molecular Weight: 191.18336
• Mol File: 138173-83-8.mol

Chemical Properties

• Boiling Point: 298.3±20.0 °C(Predicted)
• Appearance: /
• Density: 1.241
• Storage Temp.: 2-8°C
• PKA: 2.97±0.40(Predicted)
• CAS DataBase Reference: ethyl furo[2,3-c]pyridine-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl furo[2,3-c]pyridine-2-carboxylate(138173-83-8)
• EPA Substance Registry System: ethyl furo[2,3-c]pyridine-2-carboxylate(138173-83-8)

Safety Data

• Hazardous Substances Data: 138173-83-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Ethyl furo[2,3-c]pyridine-2-carboxylate is used as a synthetic intermediate for the development of new drugs. Its unique structure and reactivity allow for the creation of a variety of bioactive molecules, which can be further modified and optimized for therapeutic applications.
Used in Chemical Research:
Ethyl furo[2,3-c]pyridine-2-carboxylate is used as a research compound for studying the properties and reactivity of heterocyclic organic compounds. Its versatile functionality enables the exploration of various chemical reactions and the synthesis of novel molecules with potential applications in different fields.
Used in Agrochemical Industry:
Ethyl furo[2,3-c]pyridine-2-carboxylate is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its structure and reactivity contribute to the development of new compounds with improved efficacy and selectivity in controlling agricultural pests and weeds.
Used in Material Science:
Ethyl furo[2,3-c]pyridine-2-carboxylate is used as a building block in the development of new materials with specific properties, such as conductivity, stability, or reactivity. Its unique structure and versatility make it a valuable component in the design and synthesis of advanced materials for various applications.

Upstream product

• 106531-50-4 Ethyl 3-Hydroxyfuro<2,3-c>pyridine-2-carboxylate 
• 18343-02-7 Ethyl 2-(4-Ethoxycarbonyl-3-pyridyloxy) acetate 
• 18342-97-7 ethyl 3-hydroxyisonicotinate 
• 10128-71-9 3-hydroxyisonicotinic acid 
• 927804-63-5 ethyl 3-(((trifluoromethyl) sulfonyl)oxy)furo[2,3-c]pyridine-2-carboxylate 
• 64-17-5 ethanol 
• 112372-15-3 furo<2,3-c>pyridine-2-carboxylic acid 

Downstream Products

• 1453175-37-5 furo[2,3-c]pyridine-2-carboxylic acid 4-(1-isobutylpiperidine-4-sulfinyl)benzylamide 
• 1453173-84-6 N-[(4-tetrahydropyran-4-ylsulfonylphenyl)methyl]furo[2,3-c]pyridine-2-carboxamide 
• 1453174-07-6 N-[[4-[(1-tetrahydropyran-4-yl-4-piperidyl)sulfonyl]phenyl]methyl]furo[2,3-c]pyridine-2-carboxamide 
• 465531-08-2 furo[2,3-c]pyridine-2-carbonyl chloride 
• 1453176-78-7 furo[2,3-c]pyridine-2-carboxylic acid benzylamide 
• 1453176-79-8 4-{[(furo[2,3-c]pyridine-2-carbonyl)-amino]-methyl}-benzenesulfonyl chloride 
• 1448536-37-5 N-{[4-(piperidine-1-sulfonyl)phenyl]methyl}furo[2,3-c]pyridine-2-carboxamide 
• 1454284-75-3 N-(4-(6-methylpyridin-3-ylsulfonyl)benzyl)furo[2.3-c]pyridine-2-carboxamide 
• 1454284-57-1 furo[2,3-c]pyridine-2-carboxylic acid 4-(tetrahydropyran-4-ylsulfamoyl)benzylamide 
• 1362153-21-6 N-{[4-(benzenesulfonyl)phenyl]methyl}furo[2,3-c]pyridine-2-carboxamide 
• 1362134-17-5 N-(4-(3-(trifluoromethyl)phenylsulfonyl)benzyl)furo[2,3-c]pyridine-2-carboxamide 
• 1454250-96-4 (R)-N-([5-[(3,5-difluorobenzene)sulfinyl]pyridin-2-yl]methyl)furo[2,3-c]pyridin-2-carboxamide 
• 1454250-97-5 (S)-N-([5-[(3,5-difluorobenzene)sulfinyl]pyridin-2-yl]methyl)furo[2,3-c]pyridin-2-carboxamide 
• 1454250-93-1 N-([5-[(3,5-difluorobenzene)sulfinyl]pyridin-2-yl]methyl)furo[2,3-c]pyridin-2-carboxamide 

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Furopyridines. XI. 13C NMR Spectra of 2- or 3-Substituted Furo-, Furo- and Furopyridine

The 13C nmr spectra of 2- or 3-monosubstituted furo- 1a-1j, furo- 2a-2j, furo- 3a-3j and furopyridine derivatives 4a-4j are reported.Effects by change in annelation and substituent effects on 13C chemical shifts and carbon-proton coupling are discussed.The spectra of benzofuran derivatives 5a-5j having the corresponding substituent are also reported for comparison.