5-(2-Methylthiazol-4-yl)thiophene-2-carbaldehyde
95%
- Product Code: 48157
CAS:
499770-66-0
| Molecular Weight: | 209.29 g./mol | Molecular Formula: | C₉H₇NOS₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02682090 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its unique structure, featuring both thiazole and thiophene rings, makes it valuable for constructing heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers frequently employ it in the development of new drugs, particularly in the synthesis of compounds with potential antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the creation of diverse derivatives for screening in medicinal chemistry studies. It is also used in material science for designing organic semiconductors and conductive polymers due to its conjugated system, which can facilitate electron transport.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿16,398.00 |
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| 1.000 | 10-20 days | ฿35,055.00 |
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5-(2-Methylthiazol-4-yl)thiophene-2-carbaldehyde
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its unique structure, featuring both thiazole and thiophene rings, makes it valuable for constructing heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers frequently employ it in the development of new drugs, particularly in the synthesis of compounds with potential antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the creation of diverse derivatives for screening in medicinal chemistry studies. It is also used in material science for designing organic semiconductors and conductive polymers due to its conjugated system, which can facilitate electron transport.
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