tert-Butyl ((3-bromopyridin-2-yl)methyl)carbamate
95%
- Product Code: 36066
CAS:
1781070-64-1
| Molecular Weight: | 287.1530 g./mol | Molecular Formula: | C₁₁H₁₅BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD22199895 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of more complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a bromopyridine moiety and a carbamate protecting group, makes it valuable for constructing nitrogen-containing heterocycles, which are common in drug discovery. The compound is often utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine ring into target molecules. Additionally, the tert-butyl carbamate group can be selectively deprotected under mild conditions, allowing for further functionalization. Its applications are particularly relevant in the synthesis of compounds targeting neurological disorders, cancer, and infectious diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $305.67 |
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tert-Butyl ((3-bromopyridin-2-yl)methyl)carbamate
This chemical is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of more complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a bromopyridine moiety and a carbamate protecting group, makes it valuable for constructing nitrogen-containing heterocycles, which are common in drug discovery. The compound is often utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine ring into target molecules. Additionally, the tert-butyl carbamate group can be selectively deprotected under mild conditions, allowing for further functionalization. Its applications are particularly relevant in the synthesis of compounds targeting neurological disorders, cancer, and infectious diseases.
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