367925-74-4

Basic information

• Product Name: 5-azidomethyl-3-phenyl-1,3-oxazolidin-2-one
• Synonyms: 5-azidomethyl-3-phenyl-1,3-oxazolidin-2-one
• CAS NO: 367925-74-4
• Molecular Weight: 218.215
• Mol File: 367925-74-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 5-azidomethyl-3-phenyl-1,3-oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-azidomethyl-3-phenyl-1,3-oxazolidin-2-one(367925-74-4)
• EPA Substance Registry System: 5-azidomethyl-3-phenyl-1,3-oxazolidin-2-one(367925-74-4)

Safety Data

• Hazardous Substances Data: 367925-74-4(Hazardous Substances Data)

Upstream product

• 711-85-3 5-(chloromethyl)-3-phenyl-1,3-oxazolidin-2-one 
• 98963-12-3 5-(bromomethyl)-3-phenyloxazolidin-2-one 
• 73018-98-1 3-azidopropane-1,2-diol 
• 103-71-9 phenyl isocyanate 

Downstream Products

• 1071789-01-9 5-((4-octyl-1H-1,2,3-triazol-1-yl)methyl)-3-phenyloxazolidin-2-one 
• 1071789-03-1 3-phenyl-5-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)oxazolidin-2-one 
• 1071789-02-0 5-((4-(2-hydroxyethyl)-1H-1,2,3-triazol-1-yl)methyl)-3-phenyloxazolidin-2-one 
• 1071789-04-2 3-phenyl-5-((4-(trimethylsilyl)-1H-1,2,3-triazol-1-yl)methyl)oxazolidin-2-one 
• 121082-84-6 (l)-5-aminomethyl-3-phenyl-2-oxazolidinone 
• 96800-65-6 <3-(4-acetylphenyl)-2-oxo-5-oxazolidinyl>methyl azide 
• 367925-77-7 5-acetamidomethyl-3-phenyl-1,3-oxazolidin-2-one 

Relevant articles and documents

An approach to synthesis of 3-Aryl-2-oxazolidinones and in situ 'click' assembly of 1,2,3-triazole oxazolidinones

A facile and efficient addition of isocyanates with epoxides in the presence of MgI2 etherate was reported in good yields. The corresponding 2-oxazolidinone could be easily converted into 1,2,3-triazole-oxazolidinone by click reaction in excell

Synthesis of oxazolidinones by a solid-phase/activation cycloelimination (sp/ace) methodology

A versatile method for the solid-phase synthesis of oxazolidinones is described. An appropriate 1,2-diol is attached to immobilized sulfonyl chloride, resulting in the selective activation of one of the alcohol functions. The subsequent reaction of the ot