N-(tert-Butyl)-1H-pyrrole-2-carboxamide
95%
- Product Code: 52888
CAS:
1228957-04-7
| Molecular Weight: | 166.22 g./mol | Molecular Formula: | C₉H₁₄N₂O |
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| EC Number: | MDL Number: | MFCD16618952 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
N-(tert-Butyl)-1H-pyrrole-2-carboxamide finds its application primarily in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly those targeting neurological and inflammatory disorders. Its pyrrole ring structure makes it a valuable building block for designing molecules with potential therapeutic properties. Researchers utilize this compound in the synthesis of novel drug candidates, leveraging its ability to interact with biological targets effectively. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of new drugs. Its stability and reactivity under various conditions make it a versatile tool in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,854.00 |
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N-(tert-Butyl)-1H-pyrrole-2-carboxamide
N-(tert-Butyl)-1H-pyrrole-2-carboxamide finds its application primarily in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly those targeting neurological and inflammatory disorders. Its pyrrole ring structure makes it a valuable building block for designing molecules with potential therapeutic properties. Researchers utilize this compound in the synthesis of novel drug candidates, leveraging its ability to interact with biological targets effectively. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of new drugs. Its stability and reactivity under various conditions make it a versatile tool in medicinal chemistry and drug discovery processes.
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