124052-68-2

Basic information

• Product Name: 2,5-Furandicarboxamide(9CI)
• Synonyms: 2,5-Furandicarboxamide(9CI);2,5-Furandicarboxamide;Furan-2,5-dicarboxaMide
• CAS NO: 124052-68-2
• Molecular Formula: C₆H₆N₂O₃
• Molecular Weight: 154.12
• Product Categories: AMIDE
• Mol File: 124052-68-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Density: 1.405
• CAS DataBase Reference: 2,5-Furandicarboxamide(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Furandicarboxamide(9CI)(124052-68-2)
• EPA Substance Registry System: 2,5-Furandicarboxamide(9CI)(124052-68-2)

Safety Data

• Hazardous Substances Data: 124052-68-2(Hazardous Substances Data)

Usage

General Description

2,5-Furandicarboxamide (9CI) is a chemical compound with the molecular formula C6H6N2O3. It is also known as FDCA and is a derivative of furan, a heterocyclic organic compound. FDCA is widely used in the production of polymers and plastics as a renewable alternative to petroleum-based materials. It has also shown potential as a building block for the synthesis of biodegradable and bio-based polymers, making it an attractive option for sustainable and environmentally friendly materials. Additionally, FDCA has been studied for its potential use in pharmaceuticals, as it exhibits antimicrobial and antiviral properties. Overall, 2,5-Furandicarboxamide (9CI) plays a significant role in the development of green and sustainable chemistry.

Upstream product

• 67-47-0 5-hydroxymethyl-2-furfuraldehyde 

Downstream Products

• 58491-62-6 furan-2,5-dicarbonitrile 

Relevant articles and documents

Catalytic Amidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxamide over Alkali Manganese Oxides

2,5-Furandicarboxamide was firstly synthesized in yield of 85% via catalytic oxidative amidation of 5-hydroxymethylfurfural with aqueous NH3 over alkali manganese oxides of α-MnO2/NaxMnO2. The intermediates of 5-hydroxymethyl-furonitrile, 2,5-dicyanofuran, and 5-cyano-2-furancarboxamide were verified and their reactivities were further examined. The kinetic analysis results showed that the transformation of intermediate product of 5-cyano-2-furancarboxamide to 2,5-furan-dicarboxamide is a slower step, which is closely relative to the reaction temperature and basicity of catalyst.