25856-15-9

Basic information

• Product Name: Isoxazole, 3-(3-broMophenyl)-5-phenyl-
• Synonyms: Isoxazole, 3-(3-broMophenyl)-5-phenyl-
• CAS NO: 25856-15-9
• Molecular Formula: C₁₅H₁₀BrNO
• Molecular Weight: 300.15
• Mol File: 25856-15-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Isoxazole, 3-(3-broMophenyl)-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxazole, 3-(3-broMophenyl)-5-phenyl-(25856-15-9)
• EPA Substance Registry System: Isoxazole, 3-(3-broMophenyl)-5-phenyl-(25856-15-9)

Safety Data

• Hazardous Substances Data: 25856-15-9(Hazardous Substances Data)

Upstream product

• 25856-05-7 2,3-dibromo-1-(3-bromo-phenyl)-3-phenyl-propan-1-one 
• 86405-09-6 3-bromo-N-hydroxybenzimidoyl chloride 
• 536-74-3 phenylacetylene 
• 3132-99-8 m-bromobenzoic aldehyde 
• 53692-59-4 1-(3-bromophenyl)-3-phenylprop-2-yn-1-one 
• 1711-09-7 3-bromobenzoyl chloride 
• 22966-26-3 1-(3-bromophenyl)-3-phenylprop-2-en-1-one 

Relevant articles and documents

Aerobic oxidative synthesis of 3,5-disubstituted isoxazoles directly from α,β-unsaturated ketones

Using an efficient aerobic oxidative method, the synthesis of ten 3,5-disubstituted isoxazoles by treatment of α,β-unsaturated ketones with hydroxylamine and NaOH at room temperature has been achieved.

Simple and highly efficient synthesis of 3,5-disubstituted isoxazoles using Cu/graphene/clay nanohybrid as a new heterogeneous nano catalyst

A facile and convenient protocol for 'click' cycloaddition of structurally diverse alkynes with in situ generated nitrile oxides catalysed by Cu/aminoclay/reduced graphene oxide nanohybrid (Cu/AC/r-GO nanohybrid) as a highly efficient heterogeneous nano-c