945745-61-9

Basic information

• Product Name: 1-(4-allyloxy-3-methoxyphenyl)-3-[3-methoxy-4-(4-methoxybenzyloxy)phenyl]-4-nitrobutan-1-one
• Synonyms: 1-(4-allyloxy-3-methoxyphenyl)-3-[3-methoxy-4-(4-methoxybenzyloxy)phenyl]-4-nitrobutan-1-one
• CAS NO: 945745-61-9
• Molecular Weight: 521.567
• Mol File: 945745-61-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-allyloxy-3-methoxyphenyl)-3-[3-methoxy-4-(4-methoxybenzyloxy)phenyl]-4-nitrobutan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-allyloxy-3-methoxyphenyl)-3-[3-methoxy-4-(4-methoxybenzyloxy)phenyl]-4-nitrobutan-1-one(945745-61-9)
• EPA Substance Registry System: 1-(4-allyloxy-3-methoxyphenyl)-3-[3-methoxy-4-(4-methoxybenzyloxy)phenyl]-4-nitrobutan-1-one(945745-61-9)

Safety Data

• Hazardous Substances Data: 945745-61-9(Hazardous Substances Data)

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 75-52-5 nitromethane 
• 121-33-5 vanillin 
• 129047-38-7 3-methoxy 4-((4-methoxybenzyl)oxy)benzaldehyde 

Relevant articles and documents

Solid-supported acids as mild and versatile reagents for the deprotection of aromatic ethers

Equation Presented p-Toluene sulfonic acid (p-TsOH) immobilized either on polystyrene (PS) or silica (Si) was found to be effective in cleaving aromatic ethers containing isopropyl, tert-butyl, allyl, and benzyl groups, as well as mono-, di-, and trimethoxylated benzyl groups, in moderate to excellent yields (54-95%). These protecting groups could be selectively deprotected when they were simultaneously present on the same or different aromatic rings in a substrate.