189182-19-2

Upstream product

• 190648-31-8 tert-butyl-N-(3-trifluoroacetamidopropyl)-N-(4-trifluoroacetamidobutyl)carbamate 
• 182576-28-9 3,12-Bis-(2-nitro-benzenesulfonyl)-3,7,12,18-tetraaza-bicyclo[12.3.1]octadeca-1⁽¹⁸⁾,14,16-triene-7-carboxylic acid tert-butyl ester 
• 182576-26-7 [4-(2-Nitro-benzenesulfonylamino)-butyl]-[3-(2-nitro-benzenesulfonylamino)-propyl]-carbamic acid tert-butyl ester 
• 182576-19-8 7-(tert-butoxycarbonyl)-3,7,12,18-tetraazabicyclo[12.3.1]octadeca-1⁽¹⁸⁾,14,16-triene 
• 182576-24-5 tert butyl (4 aminobutyl)(3-aminopropyl)carbamate 
• 3958-57-4 1-bromomethyl-3-nitrobenzene 
• 158474-89-6 N-[4-(trifluoroacetamido)butyl]-N-[3-(trifluoroacetamido)propyl]amine 
• 620-13-3 1-bromomethyl-3-methyl-benzene 
• 124-20-9 N-(3-aminopropyl)-1,4-diaminobutane 
• 189182-09-0 3,12-Bis-(3-nitro-benzyl)-3,7,12,18-tetraaza-bicyclo[12.3.1]octadeca-1⁽¹⁸⁾,14,16-triene-7-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Solution phase combinatorial chemistry. Discovery of novel polyazapyridinophanes with potent antibacterial activity by a solution phase simultaneous addition of functionalities approach

Chemical modification of pre-formed asymmetric polyazaphane scaffolds by simultaneous addition of functionality (letters) in solution has been developed for the preparation of tertiary nitrogen-based combinatorial chemistry libraries. This approach has so