Methyl 3-amino-5-bromothiophene-2-carboxylate
97%
- Product Code: 117783
CAS:
107818-55-3
| Molecular Weight: | 236.09 g./mol | Molecular Formula: | C₆H₆BrNO₂S |
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| EC Number: | MDL Number: | MFCD12031265 | |
| Melting Point: | Boiling Point: | 345.5°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
Methyl 3-amino-5-bromothiophene-2-carboxylate is widely used in organic synthesis, particularly as a key intermediate in the production of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of compounds with potential therapeutic properties. It is often employed in the synthesis of heterocyclic compounds, which are essential in drug discovery for treating various diseases. Additionally, its bromine atom facilitates cross-coupling reactions, enabling the creation of complex molecules in medicinal chemistry. This chemical is also utilized in material science for designing organic electronic materials due to its thiophene backbone, which contributes to conductive properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $41.41 |
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| 0.250 | 10-20 days | $62.65 |
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| 1.000 | 10-20 days | $155.38 |
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| 5.000 | 10-20 days | $467.55 |
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Methyl 3-amino-5-bromothiophene-2-carboxylate
Methyl 3-amino-5-bromothiophene-2-carboxylate is widely used in organic synthesis, particularly as a key intermediate in the production of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of compounds with potential therapeutic properties. It is often employed in the synthesis of heterocyclic compounds, which are essential in drug discovery for treating various diseases. Additionally, its bromine atom facilitates cross-coupling reactions, enabling the creation of complex molecules in medicinal chemistry. This chemical is also utilized in material science for designing organic electronic materials due to its thiophene backbone, which contributes to conductive properties.
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