863311-15-3

Basic information

• Product Name: 3,4-Furandicarboxylic acid, 2-[(1,1-dimethylethyl)amino]-5-(4-nitrophenyl)-, 3,4-dimethyl ester
• Synonyms: 3,4-Furandicarboxylic acid, 2-[(1,1-dimethylethyl)amino]-5-(4-nitrophenyl)-, 3,4-dimethyl ester
• CAS NO: 863311-15-3
• Molecular Formula: C18H20N2O7
• Molecular Weight: 376.36
• Mol File: 863311-15-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 168-170 °C(Solv: ethanol (64-17-5))
• Boiling Point: 520.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.279±0.06 g/cm3(Predicted)
• PKA: 0.33±0.33(Predicted)
• CAS DataBase Reference: 3,4-Furandicarboxylic acid, 2-[(1,1-dimethylethyl)amino]-5-(4-nitrophenyl)-, 3,4-dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Furandicarboxylic acid, 2-[(1,1-dimethylethyl)amino]-5-(4-nitrophenyl)-, 3,4-dimethyl ester(863311-15-3)
• EPA Substance Registry System: 3,4-Furandicarboxylic acid, 2-[(1,1-dimethylethyl)amino]-5-(4-nitrophenyl)-, 3,4-dimethyl ester(863311-15-3)

Safety Data

• Hazardous Substances Data: 863311-15-3(Hazardous Substances Data)

Upstream product

• 119072-55-8 tert-butylisonitrile 
• 1198094-34-6 2-hydroxy-1-(4-nitrophenyl)-2-(4-nitrophenylamino)ethanone 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 122-04-3 4-nitro-benzoyl chloride 
• 62-23-7 4-nitro-benzoic acid 
• 555-16-8 4-nitrobenzaldehdye 

Relevant articles and documents

Competition of the R3P/DAAD and RNC/DAAD zwitterions in their production and reaction with aromatic carboxylic acids: A novel binucleophilic system for three-component synthesis of 2-aminofurans

We recently reported a new class of triphenylphosphine and isocyanide based multicomponent reactions (Ph3P/DAAD and IMCRs/DAAD) mediated by R3P/DAAD and RNC/DAAD zwitterionic intermediates in the presence of CH, OH, and NH acids. Her

A novel synthesis of aminofurans using a four-component reaction

Protonation of the reactive intermediate produced in the reaction between triphenylphosphine and dialkyl acetylenedicarboxylates by carboxylic acid leads to vinylphosphonium salts, which undergo nucleophilic reaction with carboxylate anion to produce dial

Reaction of benzoyl chlorides with Huisgen's zwitterion: synthesis of functionalized 2,5-dihydro-1H-pyrroles and tetrasubstituted furans

The 1:1 intermediate generated by the addition of alkyl(aryl) isocyanides to dimethyl acetylenedicarboxylate is trapped by benzoyl chloride to yield functionalized 2,5-dihydro-1H-pyrroles. The presence of electron-withdrawing groups at the para position o