5-Aminobenzo[b]thiophene-2-carboxylic acid
≥95%
- Product Code: 48656
CAS:
98589-46-9
| Molecular Weight: | 193.22 g./mol | Molecular Formula: | C₉H₇NO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01159705 | |
| Melting Point: | Boiling Point: | 467.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
5-Aminobenzo[b]thiophene-2-carboxylic acid is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure is particularly valuable in the development of molecules with potential therapeutic properties, such as anti-inflammatory, anticancer, and antimicrobial agents. The compound’s benzo[b]thiophene core is often incorporated into drug candidates due to its ability to interact with biological targets effectively. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex heterocyclic compounds that are essential in drug discovery and development. Its applications extend to research laboratories where it is utilized to study structure-activity relationships and optimize drug efficacy.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow powder or crystals |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft46,220.92 |
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| 0.250 | 10-20 days | Ft107,956.56 |
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5-Aminobenzo[b]thiophene-2-carboxylic acid
5-Aminobenzo[b]thiophene-2-carboxylic acid is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure is particularly valuable in the development of molecules with potential therapeutic properties, such as anti-inflammatory, anticancer, and antimicrobial agents. The compound’s benzo[b]thiophene core is often incorporated into drug candidates due to its ability to interact with biological targets effectively. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex heterocyclic compounds that are essential in drug discovery and development. Its applications extend to research laboratories where it is utilized to study structure-activity relationships and optimize drug efficacy.
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