25393-52-6

Basic information

• Product Name: 2-Oxazolidinone, 3-(4-methoxybenzoyl)-
• CAS NO: 25393-52-6
• Molecular Formula: C11H11NO4
• Molecular Weight: 221.213
• Mol File: 25393-52-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Oxazolidinone, 3-(4-methoxybenzoyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone, 3-(4-methoxybenzoyl)-(25393-52-6)
• EPA Substance Registry System: 2-Oxazolidinone, 3-(4-methoxybenzoyl)-(25393-52-6)

Safety Data

• Hazardous Substances Data: 25393-52-6(Hazardous Substances Data)

Upstream product

• 497-25-6 dimethylenecyclourethane 
• 100-07-2 4-methoxy-benzoyl chloride 
• 100-09-4 4-methoxybenzoic acid 

Downstream Products

• 2881-83-6 ethyl 4-methoxybenzoylacetate 
• 13676-94-3 2-(4-methoxyphenyl)-4,5-dihydrooxazole 
• 65908-33-0 6-methoxy-2,3-diphenyl-1H-inden-1-one 
• 611-94-9 4-Methoxybenzophenone 
• 94-30-4 ethyl 4-methoxybenzoate 
• 2280-99-1 N-butyl-p-methoxybenzamide 
• 52898-49-4 4,N-dimethoxy-N-methylbenzamide 
• 69838-98-8 1-(4-methoxybenzoyl)pyrrolidine 
• 100-09-4 4-methoxybenzoic acid 
• 6346-07-2 4-methoxy-N-(2-phenylethyl)benzamide 

Relevant articles and documents

Palladium-Catalyzed Suzuki Coupling of N-Acyloxazolidinones via Selective Cleavage of C–N Bonds

By implementing a palladium-catalyzed Suzuki coupling reaction of N-acyloxazolidinones with arylboronic acid, we herein report on the preparation of substituted diaryl ketones via selective cleavage of exocyclic C–N Bonds. The reaction was carried out under mild reaction conditions with excellent functional group compatibility in good yields (up to 93 %).

Group IV-Metal-Catalyzed Aminolysis of N-Acyl-2-oxazolidinones: Applications to the Chemoselective and Enantioselective Carbonylation of Primary Alkylamines

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