1206703-08-3

Upstream product

• 109-89-7 diethylamine 
• 90349-77-2 N-(2-nitrobenzenesulfonyl)-2-imidazolidone 

Downstream Products

• 1206703-11-8 C₂₃H₃₂N₆O₆S 
• 1206703-12-9 C₂₄H₃₄N₆O₆S 
• 1206703-13-0 C₁₈H₃₁N₅O₂ 
• 1206703-14-1 C₂₇H₄₀N₈O₇S 
• 1206703-15-2 C₃₀H₄₂N₈O₇S 
• 1206703-16-3 C₂₄H₃₉N₇O₃ 
• 1206703-10-7 C₁₄H₂₃N₃O 
• 1206703-09-4 C₂₀H₂₆N₄O₅S 

Relevant academic research and scientific papers

Synthesis of novel polymer/urea peptoid conjugates using RAFT polymerization

The synthesis of novel urea peptoids and their conjugation to polymers prepared using reversible addition-fragmentation chain transfer (RAFT) polymerization is reported. Statistical copolymers of poly(styrene-co-3- azidopropyl methacrylate) (poly(styrene-co-AzPMA)) and poly(3-O-methacryloyl1, 2: 5, 6-di-O-isopropylidene-D-glucofuranose-co-AzPMA) (poly(MAIpGlc-co-AzPMA)) were synthesized with high molecular weight and narrow molecular weight distributions. The polymer conjugates were formed using copper-catalyzed azide/alkyne cycloaddition chemistry and confirmed by FTIR and 1H NMR spectroscopy. Following conjugate formation with poly(MAIpGlc-co-AzPMA) and the urea peptoid the isopropylidene groups were removed using dilute trifluoroacetic acid. This yielded a sugar functionalized water-soluble, polymer/urea peptoid conjugate. Reactions with fluorescent compounds demonstrated that the peptoids can be further modified after conjugation to the polymer.