114372-44-0

Basic information

• Product Name: cis-5-<(4-chlorophenoxy)methyl>-3-<(1H-imidazol-1-yl)methyl>-2-methyl-3-phenylisoxazolidine
• CAS NO: 114372-44-0
• Molecular Weight: 383.878
• Mol File: 114372-44-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: cis-5-<(4-chlorophenoxy)methyl>-3-<(1H-imidazol-1-yl)methyl>-2-methyl-3-phenylisoxazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: cis-5-<(4-chlorophenoxy)methyl>-3-<(1H-imidazol-1-yl)methyl>-2-methyl-3-phenylisoxazolidine(114372-44-0)
• EPA Substance Registry System: cis-5-<(4-chlorophenoxy)methyl>-3-<(1H-imidazol-1-yl)methyl>-2-methyl-3-phenylisoxazolidine(114372-44-0)

Safety Data

• Hazardous Substances Data: 114372-44-0(Hazardous Substances Data)

Upstream product

• 13997-70-1 1-allyloxy-4-chlorobenzene 
• 119393-44-1 C₁₂H₁₃N₃O 
• 106-48-9 4-chloro-phenol 
• 24155-34-8 2-(1H-imidazol-1-yl)-1-phenylethanone 
• 4229-44-1 N-methylhydroxyamine hydrochloride 

Relevant articles and documents

1,3-Dipolar Cycloaddition Reactions of 1-Aryl-N-methyl-2-(1H-azol-1-yl)-ethanimine N-Oxides to Olefins

The regio- and stereoselectivity of the 1,3-dipolar cycloaddition reaction of 1-aryl-N-methyl-2-(1H-azol-1-yl)ethanimine N-oxides 6 to monosubstituted olefins 7 were investigated.The reaction is regioselective, leading to the corresponding C-5 substituted isoxazolidines 8/9 as cis/trans diastereomeric mixtures.The cis isomers, which are the predominant species of the mixtures, are readily separated by flash chromatography on neutral silica gel.