1429022-31-0

Basic information

• Product Name: 1-(2-(benzyloxy)-5-nitrophenyl)ethanone
• Synonyms: 1-(2-(benzyloxy)-5-nitrophenyl)ethanone
• CAS NO: 1429022-31-0
• Molecular Weight: 271.273
• Mol File: 1429022-31-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(2-(benzyloxy)-5-nitrophenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-(benzyloxy)-5-nitrophenyl)ethanone(1429022-31-0)
• EPA Substance Registry System: 1-(2-(benzyloxy)-5-nitrophenyl)ethanone(1429022-31-0)

Safety Data

• Hazardous Substances Data: 1429022-31-0(Hazardous Substances Data)

Upstream product

• 1450-76-6 1-(2-hydroxy-5-nitrophenyl)ethanone 
• 100-39-0 benzyl bromide 
• 96-97-9 5-nitrosalicylic acid 
• 100-44-7 benzyl chloride 
• 830-03-5 4-nitrophenol acetate 
• 100-02-7 4-nitro-phenol 

Downstream Products

• 1429022-37-6 N-(3-acetyl-4-(benzyloxy)phenyl)-1-naphthamide 
• 1429022-38-7 N-(3-acetyl-4-benzyloxyphenyl)nicotinamide 
• 1429022-39-8 N-(3-acetyl-4-(benzyloxy)phenyl)-2-phenylacetamide 
• 1429022-40-1 N-(3-acetyl-4-(benzyloxy)phenyl)-3-phenylpropionamide 
• 1429022-41-2 N-(3-acetyl-4-(benzyloxy)phenyl)-2-(naphthalen-1-yl)acetamide 
• 1429022-42-3 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)benzamide 
• 1429022-43-4 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)-4-chlorobenzamide 
• 1429022-44-5 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)-4-(trifluoromethyl)benzamide 
• 1429022-45-6 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)-4-methoxybenzamide 
• 1429022-46-7 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)-1-naphthamide 
• 1429022-47-8 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)nicotinamide 
• 1429022-48-9 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)-2-phenylacetamide 
• 1429022-49-0 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)-3-phenylpropanamide 
• 1429022-50-3 N-(4-(benzyloxy)-3-(2-bromoacetyl)phenyl)-2-(naphthalen-1-yl)acetamide 

Relevant articles and documents

Choline Hydroxide as a Versatile Medium for Catalyst-Free O-Functionalization of Phenols

A versatile synthetic protocol for benzyl phenyl ether preparation via O-alkylation of phenolic oxygen with readily available benzyl derivatives was demonstrated. The newly designed procedure was carried out using an eco-friendly medium, room-temperature ionic liquid (choline hydroxide), under metal- and base-catalyst-free aerobic conditions. The reaction platform was also successfully applied to phenol protection strategy.