Methyl 2-bromo-4-methylthiazole-5-carboxylate
96%
- Product Code: 43249
CAS:
81569-51-9
| Molecular Weight: | 236.0863 g./mol | Molecular Formula: | C₆H₆BrNO₂S |
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| EC Number: | MDL Number: | MFCD09998944 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a carboxylate ester group, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other biologically active compounds. Specifically, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce thiazole moieties into target molecules. Additionally, it serves as a precursor in the synthesis of thiazole-containing heterocycles, which are common in drug discovery due to their diverse pharmacological properties. Its reactivity and functional groups allow for further derivatization, enabling the creation of tailored compounds for specific applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €70.76 |
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Methyl 2-bromo-4-methylthiazole-5-carboxylate
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a carboxylate ester group, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other biologically active compounds. Specifically, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce thiazole moieties into target molecules. Additionally, it serves as a precursor in the synthesis of thiazole-containing heterocycles, which are common in drug discovery due to their diverse pharmacological properties. Its reactivity and functional groups allow for further derivatization, enabling the creation of tailored compounds for specific applications.
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