2-(Piperidin-1-yl)thiazole-4-carboxylic acid
97%
- Product Code: 115895
CAS:
952182-68-2
| Molecular Weight: | 212.27 g./mol | Molecular Formula: | C₉H₁₂N₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09027189 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its structure is often incorporated into molecules designed to interact with specific receptors in the brain, making it valuable for research into treatments for conditions like anxiety, depression, and cognitive impairments. Additionally, it is explored in the development of antimicrobial agents, leveraging its potential to disrupt bacterial or fungal growth. Researchers also investigate its role in creating novel anti-inflammatory drugs, as its scaffold can be modified to modulate inflammatory pathways effectively.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,601.00 |
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| 0.250 | 10-20 days | ฿4,545.00 |
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| 1.000 | 10-20 days | ฿11,385.00 |
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| 5.000 | 10-20 days | ฿34,983.00 |
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2-(Piperidin-1-yl)thiazole-4-carboxylic acid
This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its structure is often incorporated into molecules designed to interact with specific receptors in the brain, making it valuable for research into treatments for conditions like anxiety, depression, and cognitive impairments. Additionally, it is explored in the development of antimicrobial agents, leveraging its potential to disrupt bacterial or fungal growth. Researchers also investigate its role in creating novel anti-inflammatory drugs, as its scaffold can be modified to modulate inflammatory pathways effectively.
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