Ethyl 2-bromo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
95%
- Product Code: 43206
CAS:
150108-66-0
| Molecular Weight: | 289.1887 g./mol | Molecular Formula: | C₁₁H₁₃BrO₂S |
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| EC Number: | MDL Number: | MFCD19441937 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for creating potential drug candidates. Its structure, featuring a bromine atom and an ester group, allows for versatile reactivity, enabling modifications through various chemical reactions such as nucleophilic substitution and cross-coupling reactions. Researchers often employ it in the construction of thiophene-based molecules, which are known for their applications in pharmaceuticals, agrochemicals, and materials science. Additionally, it can serve as a precursor for the synthesis of biologically active molecules, including those with potential anti-inflammatory, antimicrobial, or anticancer properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $245.98 |
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Ethyl 2-bromo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for creating potential drug candidates. Its structure, featuring a bromine atom and an ester group, allows for versatile reactivity, enabling modifications through various chemical reactions such as nucleophilic substitution and cross-coupling reactions. Researchers often employ it in the construction of thiophene-based molecules, which are known for their applications in pharmaceuticals, agrochemicals, and materials science. Additionally, it can serve as a precursor for the synthesis of biologically active molecules, including those with potential anti-inflammatory, antimicrobial, or anticancer properties.
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