(2-Bromo-6-methoxypyridin-3-yl)methanol

≥95%

Reagent Code: #84815
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CAS Number 1807211-71-7

science Other reagents with same CAS 1807211-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.05 g/mol
Formula C₇H₈BrNO₂
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in organic synthesis as an intermediate for the production of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a bromine atom and a methoxy group, makes it a versatile reagent in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating carbon-carbon or carbon-nitrogen bonds in drug discovery. Additionally, the presence of the hydroxyl group allows for further functionalization, enabling the synthesis of derivatives with potential biological activity. It is also explored in agrochemical research for the development of novel pesticides or herbicides.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,212.00
inventory 250mg
10-20 days ฿8,433.00
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(2-Bromo-6-methoxypyridin-3-yl)methanol
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This compound is primarily used in organic synthesis as an intermediate for the production of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a bromine atom and a methoxy group, makes it a versatile reagent in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating carbon-carbon or carbon-nitroge

This compound is primarily used in organic synthesis as an intermediate for the production of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a bromine atom and a methoxy group, makes it a versatile reagent in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating carbon-carbon or carbon-nitrogen bonds in drug discovery. Additionally, the presence of the hydroxyl group allows for further functionalization, enabling the synthesis of derivatives with potential biological activity. It is also explored in agrochemical research for the development of novel pesticides or herbicides.

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