1356472-02-0

Basic information

• Product Name: 4-(4-(4-allyloxy-3-methoxybenzyloxy)-3-methoxybenzyloxy)nitrobenzene
• Synonyms: 4-(4-(4-allyloxy-3-methoxybenzyloxy)-3-methoxybenzyloxy)nitrobenzene
• CAS NO: 1356472-02-0
• Molecular Weight: 451.476
• Mol File: 1356472-02-0.mol

Chemical Properties

• CAS DataBase Reference: 4-(4-(4-allyloxy-3-methoxybenzyloxy)-3-methoxybenzyloxy)nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-(4-allyloxy-3-methoxybenzyloxy)-3-methoxybenzyloxy)nitrobenzene(1356472-02-0)
• EPA Substance Registry System: 4-(4-(4-allyloxy-3-methoxybenzyloxy)-3-methoxybenzyloxy)nitrobenzene(1356472-02-0)

Safety Data

• Hazardous Substances Data: 1356472-02-0(Hazardous Substances Data)

Upstream product

• 100-02-7 4-nitro-phenol 
• 1356472-33-7 4-(4-allyloxy-3-methoxybenzyloxy)-3-methoxybenzyl bromide 

Downstream Products

• 100-02-7 4-nitro-phenol 
• 93-51-6 2-Methoxy-4-methylphenol 
• 1356472-04-2 4-(4-(4-(4-allyloxy-3-methoxybenzyloxy)-3-methoxybenzyloxy)-3-methoxybenzyloxy)nitrobenzene 

Relevant articles and documents

Vanillin and o-vanillin oligomers as models for dendrimer disassembly

Linear analogs have been synthesized to model disassembling dendrimers. These linear analogs provide a facile synthesis to molecules that can be used to test new trigger groups and cleavage vectors. Vanillin and o-vanillin were used as the monomer units of these analogs and two trigger groups, allyl and o-nitrobenzyl, were chosen to test the disassembly process. Allyl triggered analogs 1a-d and 3a-d and o-nitrobenzyl triggered analogs 2a-c and 4a-c showed good to excellent disassembly as followed by the evolution of p-nitrophenoxide reporter ion by UV-Visible spectroscopy. The rate and yield of disassembly was shown to depend on experimental conditions as well as length of the cleavage vector.