Methyl 2-amino-4-bromothiophene-3-carboxylate
98%
- Product Code: 42656
CAS:
1239461-22-3
| Molecular Weight: | 236.0863 g./mol | Molecular Formula: | C₆H₆BrNO₂S |
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| EC Number: | MDL Number: | MFCD25956968 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both amino and bromo functional groups, makes it a valuable building block for constructing complex molecules. It is often employed in the development of heterocyclic compounds, which are crucial in drug discovery for their biological activity. Additionally, it serves as a precursor in the synthesis of thiophene-based derivatives, which are explored for their potential in materials science, particularly in the creation of organic semiconductors and conductive polymers. Its applications also extend to research settings, where it is used in the study of chemical reactions and the development of novel synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿15,849.00 |
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Methyl 2-amino-4-bromothiophene-3-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both amino and bromo functional groups, makes it a valuable building block for constructing complex molecules. It is often employed in the development of heterocyclic compounds, which are crucial in drug discovery for their biological activity. Additionally, it serves as a precursor in the synthesis of thiophene-based derivatives, which are explored for their potential in materials science, particularly in the creation of organic semiconductors and conductive polymers. Its applications also extend to research settings, where it is used in the study of chemical reactions and the development of novel synthetic pathways.
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