27409-56-9

Basic information

• Product Name: 3-(1-Hydroxy-1-methylethyl)-5-phenylisoxazole
• Synonyms: 3-(1-Hydroxy-1-methylethyl)-5-phenylisoxazole
• CAS NO: 27409-56-9
• Molecular Weight: 203.241
• Mol File: 27409-56-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(1-Hydroxy-1-methylethyl)-5-phenylisoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-Hydroxy-1-methylethyl)-5-phenylisoxazole(27409-56-9)
• EPA Substance Registry System: 3-(1-Hydroxy-1-methylethyl)-5-phenylisoxazole(27409-56-9)

Safety Data

• Hazardous Substances Data: 27409-56-9(Hazardous Substances Data)

Upstream product

• 25741-97-3 3-amino-5-methylisoxazole 
• 67-64-1 acetone 
• 55337-62-7 4-hydroxy-4-methyl-3-phenoxy-1-phenyl-pent-2-en-1-one 
• 7664-93-9 sulfuric acid 
• 536-74-3 phenylacetylene 
• 7063-99-2 ethyl 5-phenylisoxazole-3-carboxylate 
• 51060-05-0 fulminic acid 
• 74-88-4 methyl iodide 
• 75-16-1 methylmagnesium bromide 
• 917-64-6 methyl magnesium iodide 
• 74-83-9 methyl bromide 
• 7063-98-1 3-acetyl-5-phenyl-isoxazole 
• 25461-80-7 4-methyl-4-hydroxy-1-phenylpent-2-yn-1-one 

Downstream Products

• 94815-48-2 2,2-Dimethyl-5-phenyl-furan-3-ylideneamine; hydrochloride 
• 493-71-0 bullatenone 
• 110578-51-3 2,2-dimethyl-5-phenyl-furanimine hydrochloride 
• 37988-52-6 2,2-dimethyl-5-phenyl-3(2H)-furanone 
• 94815-41-5 2-penten-1-one-3-amino-4-hydroxy-4-methyl-1-phenyl 

Relevant articles and documents

Reactivity of the ester group attached isoxazoline, benzisoxazole, and isoxazole: A facial preparation of 3-acyl-substituted these heterocycles

A facile preparation of 3-acyl-substituted isoxazolines, benzisoxazoles, and isoxazoles from the corresponding 3-carboxylate esters is described. The process, involving reaction of the ester derivative of 3-carboxylic acid substituted heterocycles with Gr

ETHYL 5-SUBSTITUTED-3-ISOXAZOLECARBOXYLATES AS STARTING MATERIALS FOR A CONVENIENT ROUTE TO 3(2H)FURANONES AND 3(2H)IMINOFURANES.

Cyclodehydration of γ-hydroxy-β-enaminoketones derived from 5-substituted-3-isoxazolemethanols leads to 3(2H)furanones or 3(2H)iminofuranes depending on the substitution pattern and on the reaction conditions.