N-(4-Methoxybenzyl)isoxazol-3-amine
95%
- Product Code: 124544
CAS:
1269530-62-2
| Molecular Weight: | 204.23 g./mol | Molecular Formula: | C₁₁H₁₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD18447379 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
N-(4-Methoxybenzyl)isoxazol-3-amine finds application in the field of medicinal chemistry, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of biologically active molecules, including potential drugs targeting various diseases. Its structure is often utilized in the design of compounds with anti-inflammatory, antimicrobial, or anticancer properties. Researchers leverage its chemical framework to modify and optimize drug candidates for enhanced efficacy and selectivity. Additionally, it is employed in the study of structure-activity relationships (SAR) to understand how chemical modifications impact biological activity. This compound is also explored in the development of enzyme inhibitors, particularly those targeting specific pathways involved in disease progression. Its versatility makes it a valuable tool in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft144,092.92 |
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| 0.250 | 10-20 days | Ft270,149.98 |
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N-(4-Methoxybenzyl)isoxazol-3-amine
N-(4-Methoxybenzyl)isoxazol-3-amine finds application in the field of medicinal chemistry, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of biologically active molecules, including potential drugs targeting various diseases. Its structure is often utilized in the design of compounds with anti-inflammatory, antimicrobial, or anticancer properties. Researchers leverage its chemical framework to modify and optimize drug candidates for enhanced efficacy and selectivity. Additionally, it is employed in the study of structure-activity relationships (SAR) to understand how chemical modifications impact biological activity. This compound is also explored in the development of enzyme inhibitors, particularly those targeting specific pathways involved in disease progression. Its versatility makes it a valuable tool in drug discovery and development processes.
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