5-Bromo-3-iodo-2-methylpyridine

95%

Reagent Code: #129720
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CAS Number 1211537-13-1

science Other reagents with same CAS 1211537-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.92 g/mol
Formula C₆H₅BrIN
badge Registry Numbers
MDL Number MFCD17014993
thermostat Physical Properties
Boiling Point 270.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.171±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, 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 organic molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity or metabolic stability. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and structural properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,000.00
inventory 1g
10-20 days ฿21,600.00

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5-Bromo-3-iodo-2-methylpyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, 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 organic molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity or metabolic stability. Also utilized in agrochemical research for designing novel

Used as a key intermediate in the synthesis of pharmaceuticals, 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 organic molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity or metabolic stability. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and structural properties.

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