2-(4-Pyridyl)-1,3-thiazole-4-carboxylic acid
97%
- Product Code: 62331
CAS:
21278-86-4
| Molecular Weight: | 206.22 g./mol | Molecular Formula: | C₉H₆N₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00171745 | |
| Melting Point: | >300℃ (lit.) | Boiling Point: | 469.3±51.0℃(Predicted) |
| Density: | 1.440±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
2-(4-Pyridyl)-1,3-thiazole-4-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both pyridine and thiazole moieties, makes it a valuable scaffold for developing molecules with potential therapeutic applications. This compound is often employed in the design and synthesis of inhibitors targeting specific enzymes or receptors, particularly in the context of anti-inflammatory, antimicrobial, or anticancer drug development. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Researchers also explore its use in coordination chemistry, where it can act as a ligand to form metal complexes with potential catalytic or diagnostic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft37,914.09 |
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2-(4-Pyridyl)-1,3-thiazole-4-carboxylic acid
2-(4-Pyridyl)-1,3-thiazole-4-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both pyridine and thiazole moieties, makes it a valuable scaffold for developing molecules with potential therapeutic applications. This compound is often employed in the design and synthesis of inhibitors targeting specific enzymes or receptors, particularly in the context of anti-inflammatory, antimicrobial, or anticancer drug development. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Researchers also explore its use in coordination chemistry, where it can act as a ligand to form metal complexes with potential catalytic or diagnostic applications.
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