5-Bromo-4-iodopyridine-3-carboxylic acid

95%

Reagent Code: #146878
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CAS Number 491588-98-8

science Other reagents with same CAS 491588-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.9 g/mol
Formula C₆H₃BrINO₂
badge Registry Numbers
MDL Number MFCD11656277
thermostat Physical Properties
Melting Point 158-163°C (dec.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex pyridine-based structures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the ease of functionalization at the bromo and iodo positions. Also utilized in the preparation of ligands for catalysis and in the design of fluorescent probes or imaging agents where the carboxylic acid group can be conjugated to other molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,260.00
inventory 250mg
10-20 days ฿2,350.00
inventory 1g
10-20 days ฿9,400.00
inventory 5g
10-20 days ฿29,870.00

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5-Bromo-4-iodopyridine-3-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex pyridine-based structures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the ease of functionalization at the bromo and iodo positions. Als

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex pyridine-based structures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the ease of functionalization at the bromo and iodo positions. Also utilized in the preparation of ligands for catalysis and in the design of fluorescent probes or imaging agents where the carboxylic acid group can be conjugated to other molecules.

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