5-(p-Tolyl)furan-2-carbaldehyde
99%
- Product Code: 238107
CAS:
34035-05-7
| Molecular Weight: | 186.21 g./mol | Molecular Formula: | C₁₂H₁₀O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04084770 | |
| Melting Point: | Boiling Point: | 332.2°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its reactive aldehyde group and aromatic structure. Its furan ring and tolyl moiety make it valuable in constructing complex organic molecules, particularly in the development of bioactive compounds. Commonly employed in condensation reactions to form Schiff bases, which can exhibit antimicrobial or anticancer properties. Also utilized in materials science for the preparation of fluorescent dyes and organic semiconductors, where extended conjugation enhances electronic properties. Its versatility in cross-coupling reactions supports applications in medicinal chemistry and the design of functional organic materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $76.70 |
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| 0.100 | 10-20 days | $230.10 |
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5-(p-Tolyl)furan-2-carbaldehyde
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its reactive aldehyde group and aromatic structure. Its furan ring and tolyl moiety make it valuable in constructing complex organic molecules, particularly in the development of bioactive compounds. Commonly employed in condensation reactions to form Schiff bases, which can exhibit antimicrobial or anticancer properties. Also utilized in materials science for the preparation of fluorescent dyes and organic semiconductors, where extended conjugation enhances electronic properties. Its versatility in cross-coupling reactions supports applications in medicinal chemistry and the design of functional organic materials.
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