tert-Butyl 7-bromo-2H-benzo[b][1,4]oxazine-4(3H)-carboxylate
97%
- Product Code: 54211
CAS:
1220039-59-7
| Molecular Weight: | 314.1750 g./mol | Molecular Formula: | C₁₃H₁₆BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12913754 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of compounds with potential biological activity. The presence of the bromine atom allows for further functionalization through various coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical structures. Additionally, the tert-butyloxycarbonyl (Boc) protecting group can be selectively removed under mild acidic conditions, providing a versatile tool for stepwise synthesis in drug discovery and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,383.00 |
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tert-Butyl 7-bromo-2H-benzo[b][1,4]oxazine-4(3H)-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of compounds with potential biological activity. The presence of the bromine atom allows for further functionalization through various coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse chemical structures. Additionally, the tert-butyloxycarbonyl (Boc) protecting group can be selectively removed under mild acidic conditions, providing a versatile tool for stepwise synthesis in drug discovery and medicinal chemistry.
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