2-Bromo-3,5-dichloro-4-methylpyridine

98%

Reagent Code: #116639
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CAS Number 344324-94-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.91 g/mol
Formula C₆H₄BrCl₂N
badge Registry Numbers
MDL Number MFCD26383615
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

2-Bromo-3,5-dichloro-4-methylpyridine is primarily used as an intermediate in the synthesis of more complex chemical compounds, particularly in the pharmaceutical and agrochemical industries. Its structure allows for further functionalization, making it valuable in the development of active pharmaceutical ingredients (APIs) and crop protection agents. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create molecules with potential biological activity. Additionally, it serves as a building block in the preparation of pyridine derivatives, which are widely explored for their antimicrobial, antifungal, and herbicidal properties. Its halogenated nature also makes it useful in material science for the development of specialized polymers and coatings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days £285.76
inventory 250mg
10-20 days £95.12
inventory 100mg
10-20 days £56.95
2-Bromo-3,5-dichloro-4-methylpyridine
2-Bromo-3,5-dichloro-4-methylpyridine is primarily used as an intermediate in the synthesis of more complex chemical compounds, particularly in the pharmaceutical and agrochemical industries. Its structure allows for further functionalization, making it valuable in the development of active pharmaceutical ingredients (APIs) and crop protection agents. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create molecules with potential biological activity. Additionally, it serves as a building block in the preparation of pyridine derivatives, which are widely explored for their antimicrobial, antifungal, and herbicidal properties. Its halogenated nature also makes it useful in material science for the development of specialized polymers and coatings.
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