N-(4-(2,4-Dihydroxyphenyl)thiazol-2-yl)isobutyramide
97%
- Product Code: 52240
CAS:
1428450-95-6
Molecular Weight: | 278.3269 g./mol | Molecular Formula: | C₁₃H₁₄N₂O₃S |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a thiazole ring and dihydroxyphenyl group, makes it a valuable building block for developing compounds with potential therapeutic properties. Researchers often explore its use in designing molecules that target specific enzymes or receptors, particularly in the context of anti-inflammatory, antimicrobial, or anticancer drug development. Additionally, its unique chemical framework allows for further functionalization, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic profiles. Its applications extend to biochemical studies, where it may be used to investigate molecular interactions or mechanisms of action in biological systems.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white Solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | €37.46 |
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1.000 | 10-20 days | €142.20 |
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N-(4-(2,4-Dihydroxyphenyl)thiazol-2-yl)isobutyramide
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a thiazole ring and dihydroxyphenyl group, makes it a valuable building block for developing compounds with potential therapeutic properties. Researchers often explore its use in designing molecules that target specific enzymes or receptors, particularly in the context of anti-inflammatory, antimicrobial, or anticancer drug development. Additionally, its unique chemical framework allows for further functionalization, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic profiles. Its applications extend to biochemical studies, where it may be used to investigate molecular interactions or mechanisms of action in biological systems.
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