2-Bromo-5-iodopyrimidine
≥95%
- Product Code: 43326
CAS:
905856-70-4
| Molecular Weight: | 284.88 g./mol | Molecular Formula: | C₄H₂BrIN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18410534 | |
| Melting Point: | Boiling Point: | 341.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
2-Bromo-5-iodopyrimidine is primarily utilized in organic synthesis as a versatile building block for the construction of more complex molecules. Its structure, featuring both bromine and iodine atoms, allows for selective substitution reactions, making it valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create diverse pyrimidine derivatives. These derivatives are crucial in the design of drugs targeting various diseases, including cancer and viral infections. Additionally, it serves as an intermediate in the synthesis of nucleoside analogs, which are important in antiviral and anticancer therapies. Its reactivity and functional group compatibility make it a key reagent in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £120.30 |
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| 0.250 | 10-20 days | £240.60 |
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2-Bromo-5-iodopyrimidine
2-Bromo-5-iodopyrimidine is primarily utilized in organic synthesis as a versatile building block for the construction of more complex molecules. Its structure, featuring both bromine and iodine atoms, allows for selective substitution reactions, making it valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create diverse pyrimidine derivatives. These derivatives are crucial in the design of drugs targeting various diseases, including cancer and viral infections. Additionally, it serves as an intermediate in the synthesis of nucleoside analogs, which are important in antiviral and anticancer therapies. Its reactivity and functional group compatibility make it a key reagent in medicinal chemistry and material science research.
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