Ethyl 5-bromooxazole-4-carboxylate
95%
- Product Code: 124394
CAS:
1097306-75-6
Molecular Weight: | 220.02 g./mol | Molecular Formula: | C₆H₆BrNO₃ |
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EC Number: | MDL Number: | MFCD28137696 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
Ethyl 5-bromooxazole-4-carboxylate is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. It is often employed in the preparation of pharmaceuticals, particularly in the synthesis of heterocyclic compounds that exhibit biological activity. The bromo and ester functional groups in the molecule make it a valuable intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating diverse organic molecules. Additionally, it serves as a precursor in the synthesis of agrochemicals and other fine chemicals, where its oxazole core contributes to the desired properties of the final product. Its reactivity and structural features make it a key component in medicinal chemistry research and drug discovery processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | Ft137,693.10 |
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0.250 | 10-20 days | Ft233,884.34 |
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Ethyl 5-bromooxazole-4-carboxylate
Ethyl 5-bromooxazole-4-carboxylate is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. It is often employed in the preparation of pharmaceuticals, particularly in the synthesis of heterocyclic compounds that exhibit biological activity. The bromo and ester functional groups in the molecule make it a valuable intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating diverse organic molecules. Additionally, it serves as a precursor in the synthesis of agrochemicals and other fine chemicals, where its oxazole core contributes to the desired properties of the final product. Its reactivity and structural features make it a key component in medicinal chemistry research and drug discovery processes.
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