2-Bromo-4-chloro-5-iodopyridine
≥95%
- Product Code: 43237
CAS:
1364663-37-5
| Molecular Weight: | 318.34 g./mol | Molecular Formula: | C₅H₂BrClIN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22199250 | |
| Melting Point: | Boiling Point: | 304.4±37.0°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, protected from light and stored in an inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its unique halogen substitution pattern makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create substituted pyridine derivatives. These derivatives are often explored for their potential in pharmaceutical research, particularly in the design of drug candidates targeting various diseases. Additionally, it serves as a key intermediate in the synthesis of agrochemicals and materials with specific electronic properties. Its reactivity allows for selective functionalization, enabling researchers to tailor compounds for specific applications in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,152.00 |
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| 0.250 | 10-20 days | ฿2,502.00 |
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| 1.000 | 10-20 days | ฿8,082.00 |
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| 5.000 | 10-20 days | ฿39,951.00 |
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2-Bromo-4-chloro-5-iodopyridine
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its unique halogen substitution pattern makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create substituted pyridine derivatives. These derivatives are often explored for their potential in pharmaceutical research, particularly in the design of drug candidates targeting various diseases. Additionally, it serves as a key intermediate in the synthesis of agrochemicals and materials with specific electronic properties. Its reactivity allows for selective functionalization, enabling researchers to tailor compounds for specific applications in medicinal chemistry and material science.
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