(S)-tert-Butyl (1-(5-bromopyridin-2-yl)ethyl)carbamate
98%
- Product Code: 234968
CAS:
915720-71-7
| Molecular Weight: | 301.18 g./mol | Molecular Formula: | C₁₂H₁₇BrN₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 381.8±32.0°C | |
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its chiral structure makes it valuable for creating enantiomerically pure drugs, where the (S)-configuration is critical for biological activity. Commonly employed in medicinal chemistry for constructing pyridine-containing drug candidates, especially in oncology and inflammatory disease research. The tert-butyl carbamate (Boc) group allows for selective amine protection during multi-step syntheses, enabling controlled coupling reactions with other pharmacophores. Its bromine functionality provides a site for cross-coupling reactions such as Suzuki or Buchwald-Hartwig, facilitating rapid structural diversification in drug discovery programs.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿4,030.00 |
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| 250mg | 10-20 days | ฿12,170.00 |
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(S)-tert-Butyl (1-(5-bromopyridin-2-yl)ethyl)carbamate
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its chiral structure makes it valuable for creating enantiomerically pure drugs, where the (S)-configuration is critical for biological activity. Commonly employed in medicinal chemistry for constructing pyridine-containing drug candidates, especially in oncology and inflammatory disease research. The tert-butyl carbamate (Boc) group allows for selective amine protection during multi-step syntheses, enabling controlled coupling reactions with other pharmacophores. Its bromine functionality provides a site for cross-coupling reactions such as Suzuki or Buchwald-Hartwig, facilitating rapid structural diversification in drug discovery programs.
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