53658-17-6

Usage

Uses

Used in Pharmaceutical Industry:
(2-Hydroxyphenyl)(isoxazol-4-yl)methanone is used as an intermediate or building block for the synthesis of various pharmaceuticals due to its versatile reactivity and ability to participate in a range of chemical reactions.
Used in Agrochemical Industry:
(2-Hydroxyphenyl)(isoxazol-4-yl)methanone is also used as an intermediate or building block in the synthesis of agrochemicals, contributing to the development of new and effective products for agricultural applications.
Used in Drug Discovery and Development:
(2-HYDROXYPHENYL)(ISOXAZOL-4-YL)METHANONE's potential biological activity and unique structure make (2-Hydroxyphenyl)(isoxazol-4-yl)methanone a promising candidate for drug discovery and development, where it can be further explored for its therapeutic properties and potential applications in medicine.
Used in Organic and Medicinal Chemistry Research:
(2-Hydroxyphenyl)(isoxazol-4-yl)methanone serves as a valuable tool for research in the fields of organic and medicinal chemistry, where its unique structure and reactivity can be utilized to advance scientific understanding and develop new chemical compounds.

InChI:InChI=1/C10H7NO3/c12-9-4-2-1-3-8(9)10(13)7-5-11-14-6-7/h1-6,12H

Upstream product

• 75825-81-9 4-(o-hydroxybenzoyl)-isoxazole oxime 
• 17422-74-1 3-Formylchromone 
• 61424-75-7 3-formylchromone 3-oxime 

Downstream Products

• 91595-89-0 4-(o-hydroxybenzoyl)-pyrazolone-5 
• 75825-81-9 4-(o-hydroxybenzoyl)-isoxazole oxime 
• 1076-38-6 4-hydroxy[1]benzopyran-2-one 
• 38518-76-2 2-amino-4H-1-benzopyran-4-one 

Relevant academic research and scientific papers

Reactions of 4-Oxo-4H-1-benzopyran-3-carbaldehyde Oxime Assisted by Lanthanide(III) Cations. Roles of the Ln3+ Size, the Counterion and the Solvent.

The interaction of 4-oxo-4H-1-benzopyran-3-carbaldehyde oxime with some lanthanide(III) salts has been examined by 1H-NMR techniques.While in methanol 4-(2-hydroxybenzoyl)isoxazole is produced, in acetone 2-amino-4-oxo-4H-1-benzopyran-3-carbaldehyde and 4-oxo-4H-1-benzopyran-3-carbonitrile are formed.From the 1H-NMR data, it appears that hbisox is produced via two different pathways, depending on the lanthanide(III) used; Lu(ClO4)3 is about 4 times more reactive than LuCl3, and LaCl3 is completely ineffective, in assisting the hbisox formation; Lu3+ is about 5.5 times more effective than La3+ in assisting the formation of bpa2a and bpn.These differences in reactivity are discussed in terms of the polarizing power of the Ln3+ cation and coordinating ability of the counterion.

BENZO-γ-PYRONES.PART XII. REACTION OF 3-FORMYLCHROMONE WITH HYDROXYLAMINE

Isolation of four new derivatives of isoxazole (5) and pyrazole (7, 8, 9) formed in a reaction of 3-formylchromone (1) with hydroxylamine or as products of further transformations is described.A possible explanation for the reaction course leading to compounds 5-10 is proposed.