5-(1H-pyrazol-4-yl)furan-2-carbaldehyde
95%
- Product Code: 48114
CAS:
1934603-34-5
| Molecular Weight: | 162.15 g./mol | Molecular Formula: | C₈H₆N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22410588 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique structure, featuring both pyrazole and furan rings, makes it valuable in the design of pharmaceuticals, particularly in the synthesis of potential drug candidates targeting various diseases. Additionally, it serves as a key intermediate in the creation of heterocyclic compounds, which are often explored for their biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Its aldehyde functional group allows for further chemical modifications, enabling the attachment of various substituents to enhance its reactivity and application in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,872.00 |
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| 0.250 | 10-20 days | ฿19,818.00 |
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5-(1H-pyrazol-4-yl)furan-2-carbaldehyde
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique structure, featuring both pyrazole and furan rings, makes it valuable in the design of pharmaceuticals, particularly in the synthesis of potential drug candidates targeting various diseases. Additionally, it serves as a key intermediate in the creation of heterocyclic compounds, which are often explored for their biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Its aldehyde functional group allows for further chemical modifications, enabling the attachment of various substituents to enhance its reactivity and application in medicinal chemistry.
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