1-(Isoxazol-3-yl)ethanone

≥95%

Reagent Code: #200262
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CAS Number 88511-37-9

science Other reagents with same CAS 88511-37-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 111.10 g/mol
Formula C₅H₅NO₂
badge Registry Numbers
MDL Number MFCD16619202
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of isoxazole-containing compounds which exhibit biological activity. It serves as a building block in the development of herbicides and fungicides due to the isoxazole ring’s stability and reactivity. Also employed in medicinal chemistry for constructing heterocyclic scaffolds that are explored for anti-inflammatory and antimicrobial properties. Its ketone functionality allows for further derivatization, enabling the creation of more complex molecules in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,300.00
inventory 250mg
10-20 days ฿35,150.00
inventory 1g
10-20 days ฿84,400.00
1-(Isoxazol-3-yl)ethanone
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of isoxazole-containing compounds which exhibit biological activity. It serves as a building block in the development of herbicides and fungicides due to the isoxazole ring’s stability and reactivity. Also employed in medicinal chemistry for constructing heterocyclic scaffolds that are explored for anti-inflammatory and antimicrobial properties. Its ketone functionality allows for further der

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of isoxazole-containing compounds which exhibit biological activity. It serves as a building block in the development of herbicides and fungicides due to the isoxazole ring’s stability and reactivity. Also employed in medicinal chemistry for constructing heterocyclic scaffolds that are explored for anti-inflammatory and antimicrobial properties. Its ketone functionality allows for further derivatization, enabling the creation of more complex molecules in research and industrial applications.

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