Description

N,N’-Difurfuryloxamide (CAS No. 69010-90-8) is a high-purity organic compound with the molecular formula C₁₂H₁₂N₂O₄, widely utilized in advanced chemical research and specialty synthesis. This compound, also known by its IUPAC name N,N’-bis(furan-2-ylmethyl)oxamide, features a unique oxamide core flanked by furfuryl groups, making it a valuable intermediate for heterocyclic chemistry and polymer applications. Its well-defined structure and reactivity enable precise modifications in pharmaceutical, agrochemical, and materials science research. Supplied as a fine crystalline powder with ≥95% purity, it is rigorously tested via HPLC, NMR, and mass spectrometry to ensure batch consistency. Ideal for controlled reactions, this product is packaged under inert conditions to guarantee stability and longevity.

Properties

• CAS Number: 69010-90-8
• Complexity: 278
• IUPAC Name: N,N’-bis(2-furylmethyl)oxamide
• InChI: InChI=1S/C12H12N2O4/c15-11(13-7-9-3-1-5-17-9)12(16)14-8-10-4-2-6-18-10/h1-6H,7-8H2,(H,13,15)(H,14,16)
• InChI Key: XRURWFXKCKASSN-UHFFFAOYSA-N
• Exact Mass: 248.07970687
• Molecular Formula: C12H12N2O4
• Molecular Weight: 248.23
• SMILES: C1=COC(=C1)CNC(=O)C(=O)NCC2=CC=CO2
• Topological: 84.5
• Monoisotopic Mass: 248.07970687
• Synonyms: N,N’-DIFURFURYLOXAMIDE, 669-088-1, 69010-90-8, N,N’-bis(furan-2-ylmethyl)oxamide, N1,N2-Bis(furan-2-ylmethyl)oxalamide, BFMO, MFCD00090454, STK051972, N,N’-bis(furan-2-ylmethyl)ethanediamide, NSC320224, SCHEMBL18415483, DTXSID00317766, BCP32883, UCA01090, N1,N2-Bis(2-furylmethyl)oxalamide, AKOS000600600, HY-W054259, NSC-320224, SB60875, AS-61531, SY293311, N,N’-bis[(furan-2-yl)methyl]ethanediamide, CS-0047357, N1,N2-Bis(furan-2-ylmethyl)oxalamide;BFMO, ST50005701, W18734, SR-01000358368, SR-01000358368-1, Z56755596, N-(2-furylmethyl)-N’-(2-furylmethyl)ethane-1,2-diamide

Application

N,N’-Difurfuryloxamide serves as a versatile building block in organic synthesis, particularly for constructing furan-containing scaffolds in medicinal chemistry. Its bifunctional oxamide moiety enables cross-coupling reactions, facilitating the development of novel ligands or catalysts. Researchers also exploit its structural motifs in designing biodegradable polymers or supramolecular materials. In agrochemical studies, it may act as a precursor for bioactive compounds targeting pest control.

Safety and Hazards

GHS Hazard Statements

• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

• P264+P265, P280, P305+P351+P338, and P337+P317

Hazard Classes and Categories

• Eye Irrit. 2 (100%)

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