92573-11-0

Upstream product

• 1824-81-3 2-Amino-6-methylpyridine 
• 121-90-4 m-nitrobenzoic acid chloride 
• 92573-10-9 1-[[(6-methylpyrid-2-yl)amino]carbonyl]-3-nitrobenzene 

Downstream Products

• 143956-57-4 N-(6-Methyl-pyridin-2-yl)-3-((S)-2-phenyl-butyrylamino)-benzamide 
• 143956-58-5 N-(6-Methyl-pyridin-2-yl)-3-((R)-2-phenyl-butyrylamino)-benzamide 
• 1098180-67-6 C₂₂H₁₉N₃O₃ 
• 1098180-69-8 C₂₁H₁₉N₃O 
• 916335-79-0 3-[2-(3-methylbuturylamino)acetylamino]-N-(6-methylpyridin-2-yl)benzamide 
• 916335-84-7 3-(2-azidoacetylamino)-N-(6-methylpyridin-2-yl)benzamide 
• 916335-87-0 3-(2-chloroacetylamino)-N-(6-methylpyridin-2-yl)benzamide 
• 87056-12-0 3-(3-n-Butylureido)-N-(6-methyl-pyridin-2-yl)benzamide 
• 87055-70-7 N-(6-Methyl-pyridin-2-yl)-3-propionylamino-benzamide 

Relevant academic research and scientific papers

Making imines without making water - exploiting a recognition-mediated Aza-Wittig reaction

(Figure Presented) A recognition-mediated aza-Wittig reaction permits the efficient formation of an imine in dry CDCl3 from an iminophosphorane and an aldehyde. The kinetic and thermodynamic parameters for this reaction are compared with those

Three-point hydrogen bondings of carboxyl group in recognition of carboxylic acid and amino acid with designed synthetic receptors

The binding of carboxylic acids and amino acids have been reported with a series of designed synthetic receptors. The three-point binding of carboxylic acids (with receptors 2-4) has been utilised to bind acetylglycine with receptor 6.

MOLECULAR RECOGNITION: DIRECTED HYDROGEN BONDING RECEPTORS FOR ACYLAMINO ACID CARBOXYLATES

A new series of receptors for acylamino acid carboxylates has been synthesized and shown to have increased binding affinity for the substrate as the number of hydrogen bonding groups in the cavity increases.