2-(Pyridin-3-yl)thiazole-4-carboxylic acid
96%
- Product Code: 41473
CAS:
39067-29-3
| Molecular Weight: | 206.2211 g./mol | Molecular Formula: | C₉H₆N₂O₂S |
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| EC Number: | MDL Number: | MFCD00052304 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
2-(Pyridin-3-yl)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. It is often employed in the design and synthesis of drug candidates targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, antimicrobial, and anticancer agents. 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 complexes with metal ions, which may have applications in catalysis or material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $66.89 |
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2-(Pyridin-3-yl)thiazole-4-carboxylic acid
2-(Pyridin-3-yl)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. It is often employed in the design and synthesis of drug candidates targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, antimicrobial, and anticancer agents. 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 complexes with metal ions, which may have applications in catalysis or material science.
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