Thiophene-2,4-dicarbaldehyde
95%
- Product Code: 53674
CAS:
932-93-4
| Molecular Weight: | 140.16 g./mol | Molecular Formula: | C₆H₄O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03990651 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
Thiophene-2,4-dicarbaldehyde is primarily used in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. Its aldehyde groups make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic materials. It is often employed in the development of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its ability to enhance electronic properties. Additionally, it serves as a precursor in the synthesis of Schiff bases, which are widely studied for their potential applications in coordination chemistry, catalysis, and as bioactive agents. Its reactivity also makes it useful in the creation of complex molecular structures for research in medicinal chemistry and material science.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Pale-yellow to Yellow-brown Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,360.00 |
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| 0.250 | 10-20 days | ฿5,240.00 |
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| 1.000 | 10-20 days | ฿10,610.00 |
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Thiophene-2,4-dicarbaldehyde
Thiophene-2,4-dicarbaldehyde is primarily used in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. Its aldehyde groups make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic materials. It is often employed in the development of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its ability to enhance electronic properties. Additionally, it serves as a precursor in the synthesis of Schiff bases, which are widely studied for their potential applications in coordination chemistry, catalysis, and as bioactive agents. Its reactivity also makes it useful in the creation of complex molecular structures for research in medicinal chemistry and material science.
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