16250-89-8

Basic information

• Product Name: Oxazolidine, 2-methyl-3-phenyl-
• CAS NO: 16250-89-8
• Molecular Formula: C10H13NO
• Molecular Weight: 163.219
• Mol File: 16250-89-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Oxazolidine, 2-methyl-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazolidine, 2-methyl-3-phenyl-(16250-89-8)
• EPA Substance Registry System: Oxazolidine, 2-methyl-3-phenyl-(16250-89-8)

Safety Data

• Hazardous Substances Data: 16250-89-8(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 122-98-5 2-Anilinoethanol 
• 74-86-2 acetylene 
• 90943-43-4 N-phenylethanolamine vinyl ether 
• 71-36-3 butan-1-ol 
• 75-07-0 acetaldehyde 
• 109-92-2 ethyl vinyl ether 

Downstream Products

• 632-93-9 diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3,5-dicarboxylate 
• 124848-00-6 diethyl 2,4,6-trimethyl-1-phenyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 2506-10-7 eleagnine 

Relevant articles and documents

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The synthesis of new 1,3-oxazolidines and 1,3-oxazinanes containing (η6-arene)tricarbonylchromium group based on condensation between aldehydes and amino alcohols

The condensation reactions of β- and γ-amino alcohols containing phenyl or (η6-arene) tricarbonylchromium substituent with formaldehyde, acetaldehyde, benzaldehyde, and (η6-benzaldehyde)tricarbonylchromium were studied. The resulting 1,3-oxazolidine and 1,3-oxazinane products were isolated in a pure form and identified by different physicochemical methods. The effect of (η6-arene)tricarbonylchromium moiety on the reaction process was demonstrated.

OXAZOLIDINES. 2. SYNTHESIS OF 2-METHYLOXAZOLIDINES BY CYCLIZATION OF VINYL ETHERS OF 1,2-AMINO ALCOHOLS

A study has been made of the catalytic activity of a number of proton acids and Lewis acids, amongst which mercury salts were particularly active, in the cyclization of N-phenylethanolamine vinyl ether to 2-methyl-3-phenyloxazolidine.A method for the preparative synthesis of 2-methyloxazolidines has been developed.