2-Bromo-3,5-dichloro-4-methylpyridine
98%
- Product Code: 116639
CAS:
344324-94-3
Molecular Weight: | 240.91 g./mol | Molecular Formula: | C₆H₄BrCl₂N |
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EC Number: | MDL Number: | MFCD26383615 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, stored under inert gas |
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.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,484.00 |
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0.250 | 10-20 days | ฿4,149.00 |
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1.000 | 10-20 days | ฿12,465.00 |
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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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