6-Bromo-3-(bromomethyl)-2-methoxypyridine

95%

Reagent Code: #62871
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CAS Number 1805208-46-1

science Other reagents with same CAS 1805208-46-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.94 g/mol
Formula C₇H₇Br₂NO
badge Registry Numbers
MDL Number MFCD28733553
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both bromine substituents and a methoxy group, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in pharmaceutical and agrochemical research. The bromomethyl group allows for further functionalization, enabling the creation of diverse compounds with potential biological activity. Additionally, it serves as an intermediate in the synthesis of heterocyclic compounds, which are often explored for their therapeutic properties. Its applications extend to materials science, where it can be used to modify polymers or create specialized ligands for catalysis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,433.00
inventory 250mg
10-20 days ฿16,875.00

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6-Bromo-3-(bromomethyl)-2-methoxypyridine
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This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both bromine substituents and a methoxy group, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in pharmaceutical and agrochemical research. The bromomethyl group allows for further functionalization, enabling the creation of diverse compounds with potential biological act

This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both bromine substituents and a methoxy group, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in pharmaceutical and agrochemical research. The bromomethyl group allows for further functionalization, enabling the creation of diverse compounds with potential biological activity. Additionally, it serves as an intermediate in the synthesis of heterocyclic compounds, which are often explored for their therapeutic properties. Its applications extend to materials science, where it can be used to modify polymers or create specialized ligands for catalysis.

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