13060-78-1

Upstream product

• 698-63-5 5-nitrofurane-2-carboxaldehyde 
• 95-55-6 2-amino-phenol 
• 156-44-5 N-(5-nitrofurfurylidene)aniline 

Downstream Products

• 73315-75-0 N-(2-hydroxyphenyl)-5-nitrofurfurylamine 
• 76503-44-1 C₁₈H₁₈N₂O₅ 
• 76503-43-0 C₁₇H₁₆N₂O₅ 
• 76503-49-6 Cyclohex-1-enecarboxylic acid (2-hydroxy-phenyl)-(5-nitro-furan-2-ylmethyl)-amide 
• 76503-48-5 Cyclopent-1-enecarboxylic acid (2-hydroxy-phenyl)-(5-nitro-furan-2-ylmethyl)-amide 
• 76503-47-4 3-Methyl-but-2-enoic acid (2-hydroxy-phenyl)-(5-nitro-furan-2-ylmethyl)-amide 
• 76503-46-3 (E)-But-2-enoic acid (2-hydroxy-phenyl)-(5-nitro-furan-2-ylmethyl)-amide 
• 76503-45-2 N-(5-nitrofurfuryl)-N-(2-hydroxyphenyl)-methacrylamide 

Relevant academic research and scientific papers

SOME DATA ON THE CHEMISTRY OF 5-NITRO-2-FURALDEHYDE, V. ANILINE DERIVATIVES

UV, IR and 1H-NMR spectra of Schiff bases of 5-nitro-2-furaldehyde with mono- and disubstituted anilines have been investigated.The spectra measured in methanol, in acidic and basic media and in concentrated sulfuric acid are discussed in conne

Synthetic Control by Internal Interaction. The Intramolecular Diels-Alder Reactions of Furan Derivatives and α,β-Unsaturated Amides

An efficient method for the acceleration of the intramolecular Diels-Alder reaction was established utilizing the internal interaction - the internal hydrogen bonding and the internal coordination of a magnesium salt. The intramolecular Diels-Alder reacti