4894-24-0

Basic information

• Product Name: Isoxazole, 4,5-dihydro-5-methyl-3,5-diphenyl-
• CAS NO: 4894-24-0
• Molecular Formula: C16H15NO
• Molecular Weight: 237.301
• Mol File: 4894-24-0.mol
• Article Data: 17

Chemical Properties

• Melting Point: 78-79 °C
• Boiling Point: 352.1±45.0 °C(Predicted)
• Density: 1.07±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Isoxazole, 4,5-dihydro-5-methyl-3,5-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxazole, 4,5-dihydro-5-methyl-3,5-diphenyl-(4894-24-0)
• EPA Substance Registry System: Isoxazole, 4,5-dihydro-5-methyl-3,5-diphenyl-(4894-24-0)

Safety Data

• Hazardous Substances Data: 4894-24-0(Hazardous Substances Data)

Upstream product

• 873-67-6 benzonitrile oxide 
• 98-83-9 isopropenylbenzene 
• 611-73-4 Benzoylformic acid 
• 100-52-7 benzaldehyde 
• 1443367-86-9 1,3-diphenylbutan-1-one oxime 
• 932-90-1 Benzaldoxime 
• 495-45-4 dypnone 
• 704-18-7 2-(hydroxyimino)-2-phenylacetic acid 
• 698-16-8 benzohydroximoyl chloride 
• 622-42-4 1-nitro-1-phenylmethane 
• 14161-72-9 ((1RS,2RS)-1-methylcyclopropane-1,2-diyl)dibenzene 
• 68579-43-1 (1-methyl-2-phenylcyclopropyl)benzene 

Downstream Products

• 54435-79-9 (E)-1,3-diphenyl-3-methyl-2-propen-1-one 
• 54435-79-9 (Z)-1,3-diphenyl-2-buten-1-one 
• 62326-47-0 1,3-diphenyl-3-buten-1-one 
• 1106719-21-4 (S)-5-methyl-3,5-diphenyl-4,5-dihydroisoxazole 
• 1106719-19-0 (3S,5S)-N-benzoyl-3,5-diphenyl-5-methylisoxazolidine 
• 1106719-17-8 (3S,5R)-N-benzoyl-3,5-diphenyl-5-methylisoxazolidine 
• 2675-22-1 acetophenone p-nitrophenylhydrazone 
• 4888-37-3 N-Benzoyl-α-acetyl-β-phenyl-propylamin 
• 4888-36-2 N-Benzoyl-α-acetyl-β-methyl-β-phenyl-vinylamin 

Relevant articles and documents

TEMPO-Mediated Selective Synthesis of Isoxazolines, 5-Hydroxy-2-isoxazolines, and Isoxazoles via Aliphatic δ-C(sp3)-H Bond Oxidation of Oximes

Selective synthesis of three different bioactive heterocycles; isoxazolines, 5-hydroxy-2-isoxazolines and isoxazoles from the same starting material using TEMPO (2,2,6,6-Tetramethylpiperidin-1-oxyl) as a radical initiator is reported. Selectivity was achi

Preparation method of 4, 5-dihydroisoxazole derivative

The invention discloses a preparation method of a 4, 5-dihydroisoxazole derivative, and relates to a prepartion method of a 4, 5-dihydroisoxazole derivative represented by formula (II). The method comprises the steps: reacting hydroxylamine hydrochloride

Visible-light-mediated generation of nitrile oxides for the photoredox synthesis of isoxazolines and isoxazoles

Visible-light photoredox catalysis enables the synthesis of biologically relevant isoxazolines and isoxazoles from hydroxyimino acids. The process shows broad functional group compatibility and mechanistic and computational studies support a visible-light-mediated generation of nitrile oxides by two sequential oxidative single electron transfer processes.