17026-89-0

Basic information

• Product Name: 2-ethyl-2-methyl-1,3-oxazolidine
• Synonyms: 2-Ethyl-2-methyl-1,3-oxazolidine; Oxazolidine, 2-ethyl-2-methyl-
• CAS NO: 17026-89-0
• Molecular Formula: C₆H₁₃NO
• Molecular Weight: 115.1735
• Mol File: 17026-89-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 142.6°C at 760 mmHg
• Flash Point: 46.6°C
• Density: 0.873g/cm³
• Vapor Pressure: 5.54mmHg at 25°C
• Refractive Index: 1.411
• CAS DataBase Reference: 2-ethyl-2-methyl-1,3-oxazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ethyl-2-methyl-1,3-oxazolidine(17026-89-0)
• EPA Substance Registry System: 2-ethyl-2-methyl-1,3-oxazolidine(17026-89-0)

Safety Data

• Hazardous Substances Data: 17026-89-0(Hazardous Substances Data)

Upstream product

• 141-43-5 ethanolamine 
• 78-93-3 butanone 

Downstream Products

• 4894-06-8 3-acetyl-2-ethyl-2-methyl-oxazolidine 
• 35265-04-4 N-sec-Butylaminoethylalcohol 

Relevant articles and documents

Design, synthesis and biological activity of novel sulfonylurea oxazolidines

A series of N-[(p-methylphenyl)sulfonyl]-1,3-oxazolidine-3-carboxamide 4 was synthesized by cycloaddition and acylation reaction with alkamine, ketones, and p-methylbenzenesulfonyl isocyanate as the starting materials. The structures of all the compounds

Reductive Alkylation of β-Alkanolamines with Carbonyl Compounds and Sodium Borohydride

A synthesis of secondary alkylalkanolamines from primary alkanolamines in a rapid process in which overalkylation is virtually suppressed is described.The procedure combines the ease of formation of oxazolidines from alkanolamines with aldehydes or ketones in absolute ethanol and the lability of the newly formed C-O bond toward sodium borohydrode.The entire process is carried out in 15-35 min depending on the carbonyl substrate.