1068432-28-9

Basic information

• Product Name: methyl 2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzoate
• Synonyms: methyl 2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzoate
• CAS NO: 1068432-28-9
• Molecular Weight: 360.323
• Mol File: 1068432-28-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl 2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzoate(1068432-28-9)
• EPA Substance Registry System: methyl 2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzoate(1068432-28-9)

Safety Data

• Hazardous Substances Data: 1068432-28-9(Hazardous Substances Data)

Upstream product

• 22621-41-6 2-hydroxy-3-nitro-benzoic acid methyl ester 
• 90564-26-4 2-methoxy-3-nitro-benzoic acid methyl ester 
• 5129-25-9 2-methoxy-3-methoxycarbonylaniline 
• 40751-88-0 2-methoxy-3-nitrobenzoic acid 

Downstream Products

• 1068432-29-0 C₁₇H₁₈N₂O₅ 
• 1114333-91-3 2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzoic acid 
• 1437872-81-5 methyl 3-(3-(2-(allyloxy)-3-nitrobenzamido)-2-methoxybenzamido)-2-methoxybenzoate 
• 1437872-82-6 methyl 3-(3-(2-(allyloxy)-3-(2-methoxy-3-nitrobenzamido)benzamido)-2-methoxybenzamido)-2-methoxybenzoate 
• 1437872-83-7 methyl 3-(3-(2-(allyloxy)-3-(2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzamido)benzamido)-2-methoxybenzamido)-2-methoxybenzoate 
• 1437872-75-7 methyl 3-(3-(2-hydroxy-3-(2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzamido)benzamido)-2-methoxybenzamido)-2-methoxybenzoate 

Relevant articles and documents

Patterned recognition of amines and ammonium ions by a stimuli-responsive foldamer-based hexameric oligophenol host

A stimuli-responsive hexameric oligophenol host undergoes amine-induced co-operative folding from a more fluorescent, more linear structure into less fluorescent, more curved or helically folded states, enabling easy identification and classification of the bound amine guests. The Royal Society of Chemistry 2013.

Persistently folded circular aromatic amide pentamers containing modularly tunable cation-binding cavities with high ion selectivity

In this work, we illustrated a novel design strategy that allows systematically tunable interior properties (effective cavity size, steric crowdedness, and hydrophobicity) contained within a novel class of shape-persistent aromatic pentamers to take place on a scale below 3 A. Such finely tunable structural features are complimented by experimentally observable functional variations in ion-binding potential. Results of the selective, differential binding affinities of three circular pentamers for Li+, Na+, K+, Rb+, and Cs +, substantiated by metal-containing crystal structures and computational modeling, are detailed.

Crystallographic evidence of an unusual, pentagon-shaped folding pattern in a circular aromatic pentamer

(Figure Presented) Introduction of a continuous hydrogen-bonding network suppressed the conformational flexibility of an oligomeric backbone. Cyclization of a rigidified, suitably sized oligomer led to a circular aromatic pentamer. Its crystal structure d