CymitQuimica logo

CAS 1076-59-1

:

3-Phenyl-5(4H)-isoxazolone

Description:
3-Phenyl-5(4H)-isoxazolone, with the CAS number 1076-59-1, is an organic compound characterized by its isoxazolone structure, which features a five-membered ring containing both nitrogen and oxygen atoms. This compound typically exhibits a pale yellow to light brown appearance and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of the phenyl group contributes to its aromatic properties, influencing its reactivity and solubility in organic solvents. 3-Phenyl-5(4H)-isoxazolone can participate in various chemical reactions, such as cyclization and condensation, making it a versatile intermediate in synthetic organic chemistry. Additionally, it may exhibit biological activity, which has led to interest in its use as a building block for drug development. Its stability and reactivity can be influenced by factors such as pH and temperature, which are important considerations in its handling and application. Overall, this compound represents a significant class of heterocyclic compounds with diverse chemical properties and potential uses.
Formula:C9H7NO2
InChI:InChI=1S/C9H7NO2/c11-9-6-8(10-12-9)7-4-2-1-3-5-7/h1-5H,6H2
InChI key:InChIKey=IHKNLPPRTQQACK-UHFFFAOYSA-N
SMILES:O=C1CC(=NO1)C2=CC=CC=C2
Synonyms:
  • 2-Isoxazolin-5-one, 3-phenyl-
  • 3-Phenyl-2-isoxazolin-5-one
  • 3-Phenyl-4,5-dihydro-1,2-oxazol-5-one
  • 3-Phenyl-4,5-dihydroisoxazol-5-one
  • 3-Phenyl-4H-1,2-oxazol-5-one
  • 3-Phenyl-5(4H)-isoxazolone
  • 3-Phenyl-Δ<sup>2</sup>-5-isoxazolinone
  • 3-phenyl-1,2-oxazol-5(2H)-one
  • 3-phenyl-1,2-oxazol-5(4H)-one
  • 4,5-Dihydro-3-Phenylisoxazol-5-One
  • See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.