6-Bromo-3-iodo-2-methylpyridine

97%

Reagent Code: #151180
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CAS Number 1065483-59-1

science Other reagents with same CAS 1065483-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.92 g/mol
Formula C₆H₅BrIN
badge Registry Numbers
MDL Number MFCD11100952
thermostat Physical Properties
Boiling Point 282 °C
inventory_2 Storage & Handling
Density 2.171 g/cm3
Storage Room temperature, seal, 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 organic molecules. Commonly employed in research and development for drug discovery due to its versatility in forming carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of functionalized pyridine derivatives that serve as building blocks in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,800.00
inventory 1g
10-20 days ฿26,470.00

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6-Bromo-3-iodo-2-methylpyridine
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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 organic molecules. Commonly employed in research and development for drug discovery due to its versatility in forming carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparati

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 organic molecules. Commonly employed in research and development for drug discovery due to its versatility in forming carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of functionalized pyridine derivatives that serve as building blocks in medicinal chemistry.

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