503590-46-3

Basic information

• Product Name: 2-Oxazolidinone, 3-ethynyl-4-phenyl-, (4R)-
• CAS NO: 503590-46-3
• Molecular Formula: C11H9NO2
• Molecular Weight: 187.198
• Mol File: 503590-46-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Oxazolidinone, 3-ethynyl-4-phenyl-, (4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone, 3-ethynyl-4-phenyl-, (4R)-(503590-46-3)
• EPA Substance Registry System: 2-Oxazolidinone, 3-ethynyl-4-phenyl-, (4R)-(503590-46-3)

Safety Data

• Hazardous Substances Data: 503590-46-3(Hazardous Substances Data)

Upstream product

• 75-35-4 1,1-Dichloroethylene 
• 90319-52-1 (4R)-phenyl-2-oxazolidinone 
• 503590-28-1 (R)-4-phenyl-3-(2-triisopropylsilylethynyl)oxazolidin-2-one 
• 593-61-3 bromoethyne 

Downstream Products

• 425605-13-6 (R)-4-phenyl-3-(2-phenylethynyl)oxazolidin-2-one 
• 737004-78-3 (R)-3-(2-Methoxy-phenylethynyl)-4-phenyl-oxazolidin-2-one 
• 1190202-40-4 C₁₅H₁₅NO₄ 
• 1190202-42-6 C₁₉H₂₁NO₆ 
• 1190202-53-9 C₁₆H₁₅NO₅ 
• 1190202-43-7 C₁₆H₁₅NO₆ 
• 1190202-51-7 C₁₇H₁₅NO₄ 
• 1433810-88-8 C₂₂H₂₄N₂O₃S 
• 1433810-95-7 C₂₂H₂₄N₂O₃S 
• 1040389-77-2 C₂₄H₂₀N₂O₃ 
• 1040389-81-8 C₂₈H₂₂N₂O₃ 
• 1040389-80-7 C₂₄H₁₉BrN₂O₃ 
• 1040389-86-3 C₂₇H₂₄N₂O₅ 
• 1040389-82-9 C₂₆H₂₂N₂O₃ 

Relevant articles and documents

A Robust One-Step Approach to Ynamides

A robust one-step synthetic strategy for ynamide with cheap and easily available stock chemicals vinyl dichlorides and electron deficient amides as the starting material is described. In the absence of transition-metal catalyst, the reaction proceeds under mild reaction conditions in open air and thus rendering a convenient operation. This strategy is not only suitable for both terminal and internal ynamide synthesis but also amenable for large-scale preparation. Broad substrate scopes with respect to vinyl dichloride as well as electron-deficient amide were observed.

New stannyl enamides

New stannyl enamines derived from N-ethynyl oxazolidin-2-ones have been obtained. We describe for the first time the preparation of N-ethynyl oxazolidin-2-ones using trimethylsilylethynyl iodonium triflate. The first results of transmetallation and quenching experiments with prochiral carbonyl derivatives to give β-amino alcohols are also described.