7-Aminothieno[2,3-b]pyrazine-6-carboxylic acid
95%
- Product Code: 86868
CAS:
56881-31-3
| Molecular Weight: | 195.20 g./mol | Molecular Formula: | C₇H₅N₃O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08271964 | |
| Melting Point: | 250 °C | Boiling Point: | 464.97 °C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzymes or receptors. Its structure is advantageous for developing potential drug candidates, especially in the design of kinase inhibitors, which are crucial in treating diseases like cancer. Researchers also explore its use in creating novel heterocyclic compounds with potential therapeutic applications, such as anti-inflammatory or antimicrobial agents. Its unique thienopyrazine core makes it a valuable building block in organic synthesis for developing new molecules with diverse pharmacological properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,159.00 |
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| 0.250 | 10-20 days | ฿5,148.00 |
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| 1.000 | 10-20 days | ฿10,296.00 |
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7-Aminothieno[2,3-b]pyrazine-6-carboxylic acid
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzymes or receptors. Its structure is advantageous for developing potential drug candidates, especially in the design of kinase inhibitors, which are crucial in treating diseases like cancer. Researchers also explore its use in creating novel heterocyclic compounds with potential therapeutic applications, such as anti-inflammatory or antimicrobial agents. Its unique thienopyrazine core makes it a valuable building block in organic synthesis for developing new molecules with diverse pharmacological properties.
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