3-Iodo-6-methylpyridin-2-amine

95%

Reagent Code: #199600
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CAS Number 884495-19-6

science Other reagents with same CAS 884495-19-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.04 g/mol
Formula C₆H₇IN₂
badge Registry Numbers
MDL Number MFCD08277263
thermostat Physical Properties
Boiling Point 275.874ºC
inventory_2 Storage & Handling
Density 1.898g/cm3
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with targeted biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to build complex heterocyclic systems found in drug candidates. Also utilized in research settings for labeling and tracer studies due to the presence of iodine, which can be substituted with radioactive isotopes for imaging or mechanistic investigations.

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

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3-Iodo-6-methylpyridin-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with targeted biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to build complex heterocyclic systems found in drug candidates. Also utilized in research settings for labeling and tracer s

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with targeted biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to build complex heterocyclic systems found in drug candidates. Also utilized in research settings for labeling and tracer studies due to the presence of iodine, which can be substituted with radioactive isotopes for imaging or mechanistic investigations.

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