53573-21-0

Basic information

• Product Name: Isoxazole, 3-(4-broMophenyl)-5-phenyl-
• Synonyms: Isoxazole, 3-(4-broMophenyl)-5-phenyl-
• CAS NO: 53573-21-0
• Molecular Formula: C₁₅H₁₀BrNO
• Molecular Weight: 300.15
• Mol File: 53573-21-0.mol
• Article Data: 15

Chemical Properties

• Melting Point: 178-179 °C
• Boiling Point: 440.1±30.0 °C(Predicted)
• Appearance: /
• Density: 1.414±0.06 g/cm3(Predicted)
• PKA: -3.38±0.25(Predicted)
• CAS DataBase Reference: Isoxazole, 3-(4-broMophenyl)-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxazole, 3-(4-broMophenyl)-5-phenyl-(53573-21-0)
• EPA Substance Registry System: Isoxazole, 3-(4-broMophenyl)-5-phenyl-(53573-21-0)

Safety Data

• Hazardous Substances Data: 53573-21-0(Hazardous Substances Data)

Upstream product

• 112853-66-4 (4S,5S)-3-(4-Bromo-phenyl)-4-nitro-5-phenyl-4,5-dihydro-isoxazole 
• 67-56-1 methanol 
• 25856-01-3 1-(4-bromophenyl)-3-phenylpropane-1,3-dione 
• 7732-18-5 water 
• 536-74-3 phenylacetylene 
• 29203-58-5 4-bromo-N-hydroxybenzenecarboximidoyl chloride 
• 1774-66-9 3-(4-bromophenyl)-1-phenylprop-2-en-1-one 
• 1122-91-4 4-bromo-benzaldehyde 
• 14525-88-3 1-(4-bromophenyl)-2-phenylcyclopropane 
• 21067-52-7 4'-Brom-chalkonoxim 
• 2403-27-2 1-(4-bromophenyl)-3-phenyl-2-propen-1-one 
• 72758-69-1 (E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one 
• 112853-66-4 (4S,5R)-3-(4-Bromo-phenyl)-4-nitro-5-phenyl-4,5-dihydro-isoxazole 
• 14525-88-3 trans-1-(p-bromophenyl)-2-phenylcyclopropane 

Downstream Products

• 1133827-60-7 5-phenyl-3-[4-(phenylethynyl)phenyl]isoxazole 
• 80223-05-8 3-(4-Bromo-phenyl)-2-methyl-5-phenyl-isoxazol-2-ium; iodide 

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

Trichloroisocyanuric acid mediated one-pot synthesis of 3,5-diarylisoxazoles from α,β-unsaturated ketones

A facile one-pot synthesis of 3,5-diarylisoxazoles from α,β-unsaturated ketones and hydroxylamine hydrochloride is reported. The reaction is efficiently promoted by trichloroisocyanuric acid (TCCA) to afford the desired products, mostly in high yields and

A Copper-Catalyzed Synthesis of Pyrroles through Photochemically Generated Acylazirines

A synthesis of highly substituted 2,4-diacylpyrroles through a Cu-catalyzed dimerization of acylazirines generated in situ by a photochemical valence isomerization is described. The shown methodology allows the use of simple precursors and a readily avail