3383-42-4

Basic information

• Product Name: 5-(4-NITROPHENYL)ISOXAZOLE
• Synonyms: BUTTPARK 32\03-41;5-(4-NITROPHENYL)ISOXAZOLE
• CAS NO: 3383-42-4
• Molecular Formula: C₉H₆N₂O₃
• Molecular Weight: 190.16
• Mol File: 3383-42-4.mol

Chemical Properties

• Boiling Point: 371.2°Cat760mmHg
• Flash Point: 178.3°C
• Appearance: /
• Density: 1.333g/cm³
• Vapor Pressure: 2.24E-05mmHg at 25°C
• Refractive Index: 1.584
• CAS DataBase Reference: 5-(4-NITROPHENYL)ISOXAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-NITROPHENYL)ISOXAZOLE(3383-42-4)
• EPA Substance Registry System: 5-(4-NITROPHENYL)ISOXAZOLE(3383-42-4)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 3383-42-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research:
5-(4-NITROPHENYL)ISOXAZOLE is used as a building block for the synthesis of various organic and pharmaceutical compounds. Its unique structure allows it to be a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Synthesis Research:
In the field of organic synthesis, 5-(4-NITROPHENYL)ISOXAZOLE is used as a key intermediate for the preparation of complex organic molecules. Its reactivity and functional groups make it suitable for various synthetic pathways and reactions.
Used in Biological Activity Studies:
5-(4-NITROPHENYL)ISOXAZOLE is used as a subject of interest for studying its potential biological activities or pharmacological effects. Its unique chemical properties may contribute to the discovery of new biological targets and therapeutic applications.
Used in Chemical Compound Development:
In the chemical industry, 5-(4-NITROPHENYL)ISOXAZOLE is used for the development of new chemical compounds with specific properties. Its versatility in chemical reactions and potential for modification make it a valuable asset in creating novel compounds for various applications.

InChI:InChI=1/C9H6N2O3/c12-11(13)8-3-1-7(2-4-8)9-5-6-10-14-9/h1-6H

Upstream product

• 1006-67-3 5-phenylisoxazole 
• 15787-87-8 3-chloro-1-(4-nitro-phenyl)-propenone 
• 91869-74-8 3-(4-Nitro-phenyl)-3-[(E)-2-oxo-4,6-diphenyl-2H-pyridin-1-ylimino]-propionaldehyde oxime 
• 78089-99-3 (E)-3-dimethylamino-1-(4-nitrophenyl)-2-propen-1-one 
• 1201-93-0 1-phenyl-3-dimethylaminoprop-2-enone 
• 91869-61-3 1-[(E)-3-Dimethylamino-1-(4-nitro-phenyl)-prop-2-en-(E)-ylideneamino]-4,6-diphenyl-1H-pyridin-2-one 

Downstream Products

• 3383-40-2 4-nitro-5-(4-nitro-phenyl)-isoxazole 

Relevant articles and documents

A novel synthesis of 5-substituted isoxazoles from propargylic amines and N-hydroxyphthalimide

A mild and efficient method for the synthesis of 5-substituted isoxazoles through cyclization of propargylic amines with N-hydroxyphthalimide (NHPI) under metal-free conditions was developed.

Reaction of β-dimethylaminovinyl ketones with hydroxylamine: A simple and useful method for synthesis of 3- and 5-substituted isoxazoles

(Chemical Equation Presented) The regioselective synthesis of 3- and 5-substituted-isoxazoles from the reaction of β-dimethylaminovinyl ketones [R-C(O)CH=CH-NMe2, where R = Ph, MeO-4-C6H4, F-4-C6H4, C

New Synthesis of Pyrazole and Isoxazole Derivatives

A convenient synthesis of 5-aryl-1-phenylpyrazoles and 5-arylisoxazoles, from readily available ketimine 1 dimethylformamide dimethylacetal and phenylhydrazine or hydroxylamine, is described.