2-(Pyridin-4-yl)thiazole-5-carbaldehyde
98%
- Product Code: 96649
CAS:
21346-36-1
| Molecular Weight: | 190.22 g./mol | Molecular Formula: | C₉H₆N₂OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11846891 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a pyridine and a thiazole ring, makes it particularly valuable in the synthesis of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers frequently employ it in the creation of novel drug candidates, especially in the development of compounds targeting neurological disorders and infectious diseases. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives that can exhibit diverse biological properties. Beyond pharmaceutical applications, it is also investigated in material science for the design of organic semiconductors and light-emitting materials due to its conjugated system and electron-rich nature.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,160.00 |
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| 0.250 | 10-20 days | ฿23,040.00 |
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2-(Pyridin-4-yl)thiazole-5-carbaldehyde
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a pyridine and a thiazole ring, makes it particularly valuable in the synthesis of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers frequently employ it in the creation of novel drug candidates, especially in the development of compounds targeting neurological disorders and infectious diseases. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives that can exhibit diverse biological properties. Beyond pharmaceutical applications, it is also investigated in material science for the design of organic semiconductors and light-emitting materials due to its conjugated system and electron-rich nature.
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