tert-Butyl 2-bromo-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate
≥95%
- Product Code: 116747
CAS:
365996-06-1
| Molecular Weight: | 319.22 g./mol | Molecular Formula: | C₁₁H₁₅BrN₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09951958 | |
| Melting Point: | Boiling Point: | 390.946°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the construction of heterocyclic compounds, particularly those with thiazolo[5,4-c]pyridine frameworks, which are of interest in medicinal chemistry. Its structure allows for further functionalization, making it valuable in the synthesis of potential drug candidates, especially in the areas of kinase inhibitors and other biologically active molecules. The tert-butyl group provides steric protection, enabling selective reactions at other sites of the molecule. Additionally, the bromo substituent offers a reactive handle for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, facilitating the introduction of diverse substituents. This versatility makes it a useful building block in the discovery and optimization of pharmaceuticals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,233.00 |
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| 1.000 | 10-20 days | ฿3,042.00 |
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| 5.000 | 10-20 days | ฿9,072.00 |
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| 10.000 | 10-20 days | ฿16,515.00 |
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tert-Butyl 2-bromo-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the construction of heterocyclic compounds, particularly those with thiazolo[5,4-c]pyridine frameworks, which are of interest in medicinal chemistry. Its structure allows for further functionalization, making it valuable in the synthesis of potential drug candidates, especially in the areas of kinase inhibitors and other biologically active molecules. The tert-butyl group provides steric protection, enabling selective reactions at other sites of the molecule. Additionally, the bromo substituent offers a reactive handle for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, facilitating the introduction of diverse substituents. This versatility makes it a useful building block in the discovery and optimization of pharmaceuticals.
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