tert-Butyl ((6-bromopyridin-2-yl)methyl)carbamate
97%
- Product Code: 36088
CAS:
887580-31-6
| Molecular Weight: | 287.1530 g./mol | Molecular Formula: | C₁₁H₁₅BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD07367931 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
tert-Butyl ((6-bromopyridin-2-yl)methyl)carbamate is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key building block for the development of more complex molecules, often utilized in the synthesis of active pharmaceutical ingredients (APIs) or biologically active compounds. The bromine atom on the pyridine ring makes it a versatile reagent for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical structures. Additionally, the carbamate group provides a protective function for amines during multi-step synthetic processes, ensuring selective reactivity in complex transformations. Its applications are particularly relevant in the design of drugs targeting neurological disorders, inflammation, or infectious diseases, where pyridine derivatives play a significant role.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $171.18 |
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tert-Butyl ((6-bromopyridin-2-yl)methyl)carbamate
tert-Butyl ((6-bromopyridin-2-yl)methyl)carbamate is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key building block for the development of more complex molecules, often utilized in the synthesis of active pharmaceutical ingredients (APIs) or biologically active compounds. The bromine atom on the pyridine ring makes it a versatile reagent for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical structures. Additionally, the carbamate group provides a protective function for amines during multi-step synthetic processes, ensuring selective reactivity in complex transformations. Its applications are particularly relevant in the design of drugs targeting neurological disorders, inflammation, or infectious diseases, where pyridine derivatives play a significant role.
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