3-(4-Bromophenyl)isoxazole

≥95%

Reagent Code: #117453
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CAS Number 13484-04-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.05 g/mol
Formula C₉H₆BrNO
badge Registry Numbers
MDL Number MFCD08446384
thermostat Physical Properties
Melting Point 99-104°C
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring an isoxazole ring and a bromophenyl group, makes it a valuable building block for creating more complex molecules. In medicinal chemistry, it is often employed in the development of compounds with potential biological activities, such as anti-inflammatory, antimicrobial, or anticancer agents. The bromine atom on the phenyl ring allows for further functionalization through cross-coupling reactions, enabling the synthesis of diverse derivatives for drug discovery. Additionally, it finds application in material science, particularly in the synthesis of organic electronic materials. Its aromatic and heterocyclic components contribute to the development of organic semiconductors or light-emitting materials used in electronic devices. Overall, its versatility in chemical reactions and structural features make it a valuable component in both pharmaceutical and material science research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,998.00
inventory 1g
10-20 days ฿4,986.00
inventory 5g
10-20 days ฿16,542.00
inventory 10g
10-20 days ฿27,585.00
3-(4-Bromophenyl)isoxazole
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring an isoxazole ring and a bromophenyl group, makes it a valuable building block for creating more complex molecules. In medicinal chemistry, it is often employed in the development of compounds with potential biological activities, such as anti-inflammatory, antimicrobial, or anticancer agents. The bromine atom on the phenyl ring allows for further functionalization through cross-coupling reactions, enabling the synthesis of diverse derivatives for drug discovery. Additionally, it finds application in material science, particularly in the synthesis of organic electronic materials. Its aromatic and heterocyclic components contribute to the development of organic semiconductors or light-emitting materials used in electronic devices. Overall, its versatility in chemical reactions and structural features make it a valuable component in both pharmaceutical and material science research.
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