5-(3-Bromophenyl)isoxazole

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Reagent Code: #48194
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CAS Number 7064-33-7

science Other reagents with same CAS 7064-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.0500 g/mol
Formula C₉H₆BrNO
badge Registry Numbers
MDL Number MFCD02183531
thermostat Physical Properties
Boiling Point 602 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.3g/cm3
Storage room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting neurological disorders. Its structure is valuable in developing inhibitors for enzymes involved in neurodegenerative diseases. Additionally, it serves as a building block in organic chemistry for creating complex molecules with potential therapeutic applications, such as anti-inflammatory and anticancer agents. Its bromophenyl group enhances reactivity, making it useful in cross-coupling reactions for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,917.00

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5-(3-Bromophenyl)isoxazole
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting neurological disorders. Its structure is valuable in developing inhibitors for enzymes involved in neurodegenerative diseases. Additionally, it serves as a building block in organic chemistry for creating complex molecules with potential therapeutic applications, such as anti-inflammatory and anticancer agents. Its bromophenyl group enhances reactivity, making it useful in cross-cou

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting neurological disorders. Its structure is valuable in developing inhibitors for enzymes involved in neurodegenerative diseases. Additionally, it serves as a building block in organic chemistry for creating complex molecules with potential therapeutic applications, such as anti-inflammatory and anticancer agents. Its bromophenyl group enhances reactivity, making it useful in cross-coupling reactions for drug discovery and development.

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