1325297-13-9

Basic information

• Product Name: ethyl 1-benzyl-5-(tert-butoxycarbonylamino)-4-oxo-1,4-dihydropyridine-3-carboxylate
• Synonyms: ethyl 1-benzyl-5-(tert-butoxycarbonylamino)-4-oxo-1,4-dihydropyridine-3-carboxylate
• CAS NO: 1325297-13-9
• Molecular Weight: 372.421
• Mol File: 1325297-13-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl 1-benzyl-5-(tert-butoxycarbonylamino)-4-oxo-1,4-dihydropyridine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-benzyl-5-(tert-butoxycarbonylamino)-4-oxo-1,4-dihydropyridine-3-carboxylate(1325297-13-9)
• EPA Substance Registry System: ethyl 1-benzyl-5-(tert-butoxycarbonylamino)-4-oxo-1,4-dihydropyridine-3-carboxylate(1325297-13-9)

Safety Data

• Hazardous Substances Data: 1325297-13-9(Hazardous Substances Data)

Upstream product

• 105-50-0 diethyl 1,3-acetonedicarboxylate 
• 74632-03-4 diethyl 4-oxo-1,4-dihydro-3,5-pyridinedicarboxylate 
• 100-39-0 benzyl bromide 
• 1325297-12-8 1-benzyl-5-(ethoxycarbonyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 
• 75-65-0 tert-butyl alcohol 
• 1325297-11-7 diethyl 1-benzyl-4-oxo-1,4-dihydropyridine-3,5-dicarboxylate 

Downstream Products

• 1325297-18-4 C₂₈H₂₆N₄O₅ 
• 1325297-59-3 ethyl 1-benzyl-5-(1-benzyl-5-(1-benzyl-5-(1-benzyl-5-(tert-butoxycarbonylamino)-4-oxo-1,4-dihydropyridine-3-carboxamido)-4-oxo-1,4-dihydropyridine-3-carboxamido)-4-oxo-1,4-dihydropyridine-3-carboxamido)-4-oxo-1,4-dihydropyridine-3-carboxylate 
• 1325297-14-0 1-benzyl-5-(tert-butoxycarbonylamino)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 
• 1325297-15-1 C₁₅H₁₆N₂O₃ 
• 1350912-63-8 5-amino-1-benzyl-4-oxo-1,4-dihydropyridine-3-carboxylic acid 
• 1325297-09-3 C₆₅H₅₀N₁₀O₁₀ 

Relevant articles and documents

Five-fold-symmetric macrocyclic aromatic pentamers: High-affinity cation recognition, ion-pair-induced columnar stacking, and nanofibrillation

Described in this study is a conceptually new class of five-fold-symmetric cavity-containing planar pentameric macrocycles with their interior decorated by five convergently aligned, properly spaced carbonyl oxygen atoms. These cation-binding oxygens enclose a hydrophilic lumen of 2.85 A in radius and thus display high-affinity binding toward alkali metal cations, and possibly many other cations, too. Arising from their high-affinity recognition of metal ions, these planar macrocycles form cation- or ion-pair-induced one-dimensional columnar aggregates, and subsequently fascinating fibrillation results.