73315-75-0

Upstream product

• 95-55-6 2-amino-phenol 
• 698-63-5 5-nitrofurane-2-carboxaldehyde 
• 20782-91-6 2-(bromomethyl)-5-nitrofuran 
• 13060-78-1 2-hydroxy-N-(5-nitrofurfurylidene)aniline 

Downstream Products

• 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 
• 76503-44-1 C₁₈H₁₈N₂O₅ 
• 76503-43-0 C₁₇H₁₆N₂O₅ 
• 76503-45-2 N-(5-nitrofurfuryl)-N-(2-hydroxyphenyl)-methacrylamide 
• 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 

Relevant academic research and scientific papers

ALIPHATIC AND AROMATIC 5-NITRO-2-FURYLAMINES AND AROMATIC 5-NITROFURFURYL ETHERS

Tertiary 5-nitrofurylamines were prepared by a nucleophilic substitution of 5-nitro-2-furfuryl bromide (I) with aliphatic secondary amines.According to reaction conditions N-(5-nitro-2-furfuryl)-X-phenylamines or their mixture with N,N-di(5-nitro-2-furfuryl)-X-phenylamines were obtained from the reaction of I with substituted primary aromatic amines.Compound I gave with 2-aminophenol a mixture of O- and N-mono- and disubstituted derivatives, and with ethyl salicylate ethyl 2-(5-nitro-2-furfuryloxy)benzoate.

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