Ethyl 2-amino-5-bromothiophene-3-carboxylate
≥95%
- Product Code: 116321
CAS:
56387-07-6
| Molecular Weight: | 250.11 g./mol | Molecular Formula: | C₇H₈BrNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275092 | |
| Melting Point: | Boiling Point: | 316.1±37.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
Ethyl 2-amino-5-bromothiophene-3-carboxylate is primarily used as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both amino and bromo groups, makes it a versatile building block for constructing more complex molecules. In medicinal chemistry, it is often utilized to develop compounds with potential biological activity, such as antimicrobial, anti-inflammatory, or anticancer agents. Additionally, it serves as a precursor in the synthesis of thiophene-based heterocycles, which are important in the design of dyes, pigments, and organic electronic materials. Its reactivity allows for further functionalization, enabling the creation of diverse chemical entities for research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $495.38 |
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| 0.250 | 10-20 days | $867.33 |
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| 1.000 | 10-20 days | $2,168.33 |
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Ethyl 2-amino-5-bromothiophene-3-carboxylate
Ethyl 2-amino-5-bromothiophene-3-carboxylate is primarily used as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both amino and bromo groups, makes it a versatile building block for constructing more complex molecules. In medicinal chemistry, it is often utilized to develop compounds with potential biological activity, such as antimicrobial, anti-inflammatory, or anticancer agents. Additionally, it serves as a precursor in the synthesis of thiophene-based heterocycles, which are important in the design of dyes, pigments, and organic electronic materials. Its reactivity allows for further functionalization, enabling the creation of diverse chemical entities for research and industrial applications.
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