5-(4-Methoxyphenyl)isoxazole-3-carboxaldehyde
≥95%
- Product Code: 48261
CAS:
870703-95-0
| Molecular Weight: | 203.19 g./mol | Molecular Formula: | C₁₁H₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06798096 | |
| Melting Point: | 153-157℃ (lit.) | Boiling Point: | 394.6±37.0℃(Predicted) |
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of various pharmacologically active molecules. Its structure, featuring both an isoxazole ring and a methoxyphenyl group, makes it a valuable building block for designing compounds with potential biological activities. It is often employed in the synthesis of heterocyclic compounds, which are explored for their antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it serves as a precursor in the preparation of fluorescent dyes and sensors due to its aldehyde functionality, which can be easily modified for specific applications. Its versatility in chemical reactions, such as condensation and cyclization, further enhances its utility in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿14,967.00 |
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5-(4-Methoxyphenyl)isoxazole-3-carboxaldehyde
This compound is primarily utilized in organic synthesis as a key intermediate for the development of various pharmacologically active molecules. Its structure, featuring both an isoxazole ring and a methoxyphenyl group, makes it a valuable building block for designing compounds with potential biological activities. It is often employed in the synthesis of heterocyclic compounds, which are explored for their antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it serves as a precursor in the preparation of fluorescent dyes and sensors due to its aldehyde functionality, which can be easily modified for specific applications. Its versatility in chemical reactions, such as condensation and cyclization, further enhances its utility in medicinal chemistry and material science research.
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