84403-55-4

Basic information

• Product Name: 4-(benzyloxy)-N,N-dimethylbenzamide
• Synonyms: 4-(benzyloxy)-N,N-dimethylbenzamide
• CAS NO: 84403-55-4
• Molecular Weight: 255.316
• Mol File: 84403-55-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-(benzyloxy)-N,N-dimethylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(benzyloxy)-N,N-dimethylbenzamide(84403-55-4)
• EPA Substance Registry System: 4-(benzyloxy)-N,N-dimethylbenzamide(84403-55-4)

Safety Data

• Hazardous Substances Data: 84403-55-4(Hazardous Substances Data)

Upstream product

• 20876-99-7 4-hydroxy-N,N-dimethyl-benzamide 
• 100-39-0 benzyl bromide 
• 1486-50-6 4-(benzyloxy)benzoic acid chloride 
• 124-40-3 dimethyl amine 

Downstream Products

• 1251581-55-1 C₂₂H₁₅ClO₃ 
• 20876-99-7 4-hydroxy-N,N-dimethyl-benzamide 
• 836-43-1 4-benzyloxybenzyl alcohol 
• 1251581-60-8 C₂₆H₂₂N₂O₄ 
• 1251581-64-2 C₂₃H₂₃N₃O₅ 
• 1251585-20-2 C₂₃H₂₅N₃O₄ 
• 1251581-58-4 C₂₅H₂₃NO₄ 
• 1251581-62-0 C₁₉H₁₆N₂O₄ 
• 4397-53-9 p-benzyloxybenzaldehyde 

Relevant articles and documents

A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh2andtBuOK

A general method for the demethylation, debenzylation, and deallylation of aryl ethers using HPPh2andtBuOK is reported. The reaction features mild and metal-free reaction conditions, broad substrate scope, good functional group compatibility, and high chemical selectivity towards aryl ethers over aliphatic structures. Notably, this approach is competent to selectively deprotect the allyl or benzyl group, making it a general and practical method in organic synthesis.