237435-96-0

Basic information

• Product Name: Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate
• Synonyms: Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate;3-Amino-5-(2-furyl)-1H-pyrrole-2-carboxylic acid ethyl ester
• CAS NO: 237435-96-0
• Molecular Formula: C11H12N2O3
• Molecular Weight: 220.22
• Mol File: 237435-96-0.mol

Chemical Properties

• Melting Point: 124-125℃
• Boiling Point: 436.874°C at 760 mmHg
• Flash Point: 218.014°C
• Appearance: /
• Density: 1.276
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.59
• Storage Temp.: 2-8°C
• PKA: 15.93±0.50(Predicted)
• CAS DataBase Reference: Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate(237435-96-0)
• EPA Substance Registry System: Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate(237435-96-0)

Safety Data

• Hazardous Substances Data: 237435-96-0(Hazardous Substances Data)

Usage

Uses

Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate is used as a chemical intermediate for [application reason] in the chemical industry. The presence of the carboxylate ester and amino groups in its structure suggests that it may be involved in the synthesis of more complex molecules or used in reactions that require these functional groups.
Used in Chemical Synthesis:
Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate is used as a building block for the synthesis of more complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its reactivity and the presence of functional groups make it a valuable component in the creation of new molecules with potential applications in these fields.
Used in Research Applications:
Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate is used as a research compound for studying the properties and reactions of heterocyclic aromatic compounds. Its unique structure and potential reactivity provide opportunities for researchers to explore new chemical pathways and mechanisms, contributing to the advancement of organic chemistry.

InChI:InChI=1/C11H12N2O3/c1-2-15-11(14)10-7(12)6-8(13-10)9-4-3-5-16-9/h3-6,13H,2,12H2,1H3

Upstream product

• 13433-00-6 diethyl aminomalonate hydrochloride 

Downstream Products

• 871025-06-8 6-(furan-2-yl)-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-4-one 
• 1335106-60-9 6-(2-furanyl)-3-[2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl]-1,5-dihydropyrrolo[3,2-d]pyrimidine-2,4-dione 
• 1335106-61-0 3-[2-[4-(2-chlorophenyl)piperazin-1-yl]ethyl]-6-(2-furanyl)-1,5-dihydropyrrolo[3,2-d]pyrimidine-2,4-dione 

Relevant articles and documents

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The present invention relates to a compound represented by the formula: wherein W is C(R 1 ) or N, each A is an optionally substituted aryl group or a heteroaryl group, X 1 is -NR 3 -Y 1 -, -O-, -S-, -SO-, -SO 2 or -CHR 3 - wherein R 3 is a hydrogen atom or an optionally substituted aliphatic hydrocarbon group, or R 3 is optionally bonded to A to form an optionally substituted ring structure, R 1 is a hydrogen atom or an optionally substituted group bonded via a carbon atom, a nitrogen atom or an oxygen atom, R 2 is a hydrogen atom or optionally substituted group bonded via a carbon atom or a sulfur atom, or R 1 and R 2 , or R 2 and R 3 are optionally bonded to form an optionally substituted ring structure, or a salt thereof, and a tyrosine kinase inhibitor or an agent for the prophylaxis or treatment of cancer, which contains this compound or a prodrug thereof.

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