3-Bromo-5-fluoroisonicotinamide

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Reagent Code: #145084
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CAS Number 1353636-72-2

science Other reagents with same CAS 1353636-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.01 g/mol
Formula C₆H₄BrFN₂O
thermostat Physical Properties
Boiling Point 249.6±40.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective modifications, making it valuable in creating targeted drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The compound's halogenated pyridine core enhances binding affinity in various biological systems, supporting its use in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,740.00
inventory 250mg
10-20 days ฿5,280.00

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3-Bromo-5-fluoroisonicotinamide
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective modifications, making it valuable in creating targeted drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The compound's halogenated pyridine core enhances binding affinity in various biological systems, supporting its use i

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective modifications, making it valuable in creating targeted drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The compound's halogenated pyridine core enhances binding affinity in various biological systems, supporting its use in structure-activity relationship (SAR) studies.

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