1255792-08-5

Upstream product

• 1255792-05-2 1-(5-methoxy-2-nitro-4-(prop-2-yn-1-yloxy)phenyl)ethan-1-ol 
• 1255792-04-1 1-(5-methoxy-2-nitro-4-(prop-2-yn-1-yloxy)phenyl)ethan-1-one 
• 6253-28-7 3,6-epoxy-1,2,3,6-tetrahydrophthalimide 
• 1456901-32-8 1-(5-methoxy-2-nitro-4-prop-2-ynyloxyphenyl)ethyl bromide 

Downstream Products

• 1456901-35-1 2-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione 
• 1456901-37-3 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione 
• 1456901-39-5 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-3-(octylthio)pyrrolidine-2,5-dione 

Relevant academic research and scientific papers

A heterobifunctional linker bearing azide-reactive alkyne and thiol-reactive maleimide connected with N-(2-Nitrobenzyl)imide to synthesize photocleavable diblock copolymers

A novel heterobifunctional linker 1 connected with photocleavable N-(2-nitrobenzyl)imide has been developed. Hydrophobic polystyrene (PS), hydrophilic poly(ethylene oxide) (PEO), and thermosensitive poly(N- isopropylacrylamide) (PNIPAM) containing thiol or azide at the terminal, synthesized by a living radical polymerization or a transformation of terminal functional groups, were coupled with the alkyne and maleimide protected as the furan adduct at both terminals of 1 to synthesize three types of photocleavable diblock copolymers in high yields.