4264-04-4

Basic information

• Product Name: Isoxazole, 3-(3-nitrophenyl)-
• CAS NO: 4264-04-4
• Molecular Formula: C9H6N2O3
• Molecular Weight: 190.158
• Mol File: 4264-04-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Isoxazole, 3-(3-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxazole, 3-(3-nitrophenyl)-(4264-04-4)
• EPA Substance Registry System: Isoxazole, 3-(3-nitrophenyl)-(4264-04-4)

Safety Data

• Hazardous Substances Data: 4264-04-4(Hazardous Substances Data)

Upstream product

• 112853-63-1 3-(3-nitrophenyl)-5-hydroxy-2-isoxazoline 
• 63008-30-0 3-(m-nitrophenyl)-5-nitro-4,5-dihydro-1,2-oxazole 
• 7007-35-4 m-nitrobenzonitrile oxide 
• 33341-70-7 N-chloro-3-nitro-benzamide 
• 593-60-2 Vinyl bromide 
• 3431-62-7 3-nitrobenzaldoxime 
• 3717-29-1 E-3-nitrobenzaldoxime 
• 115955-48-1 3-(dimethylamino)-1-(3-nitrophenyl)-2-propen-1-one 

Downstream Products

• 769160-19-2 3-(3-aminophenyl)isoxazole 

Relevant articles and documents

3-AZABICYCLO [3.1.0] HEXANE DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

The present invention relates to 3-azabicyclo[3.1.0]hexane derivatives, which are useful as vanilloid receptor (VR) ligands, methods of treating diseases, conditions and/or disorders modulated by vanilloid receptors with them, and processes for preparing them.

BENZIMIDAZOLE DERIVATIVES AND THEIR USE FOR MODULATING THE GABAA RECEPTOR COMPLEX

This invention relates to novel benzimidazole derivatives of formula (I), pharmaceutical compositions containing these compounds, and methods of treatment therewith. The compounds of the invention are useful in the treatment of central nervous system diseases and disorders, which are responsive to modulation of the GABAA receptor complex, and in particular for combating anxiety and related diseases.

SYNTHESIS AND PROPERTIES OF AZOLS AND THEIR DERIVATIVES. PART VI. CYCLOADDITION REACTIONS OF NITROETHYLENE WITH AROMATIC NITRILE N-OXIDES AND SOME CONVERSIONS OF 3-ARYL-5-NITRO-4,5-DIHYDRO-1,2-OXAZOLES

Reactions of aromatic nitrile N-oxides with nitroethylene lead to formation of 3-aryl-5-nitro-4,5-dihydro-1,2-oxazoles.During heating the above compounds decompose with elimination of nitrous acid, thus affording 3-aryl-1,2-oxazoles.Under nucleophilic reagents a ring opening was observed.