Ethyl 2-amino-7-((2-(tert-butoxy)-2-oxoethyl)amino)-5-fluoro-1H-indole-3-carboxylate
97%
- Product Code: 82888
CAS:
1400808-16-3
| Molecular Weight: | 351.37 g./mol | Molecular Formula: | C₁₇H₂₂FN₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28098117 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring an indole core with amino and fluoro substituents, makes it a valuable intermediate in the creation of biologically active molecules. It is often employed in the development of potential therapeutic agents targeting various diseases, including cancer, due to its ability to interact with specific biological pathways. Additionally, its ester and tert-butoxy groups enhance its reactivity, making it suitable for further chemical modifications in medicinal chemistry. Researchers also explore its use in the design of fluorescent probes or imaging agents, leveraging its indole moiety for optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $573.37 |
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Ethyl 2-amino-7-((2-(tert-butoxy)-2-oxoethyl)amino)-5-fluoro-1H-indole-3-carboxylate
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring an indole core with amino and fluoro substituents, makes it a valuable intermediate in the creation of biologically active molecules. It is often employed in the development of potential therapeutic agents targeting various diseases, including cancer, due to its ability to interact with specific biological pathways. Additionally, its ester and tert-butoxy groups enhance its reactivity, making it suitable for further chemical modifications in medicinal chemistry. Researchers also explore its use in the design of fluorescent probes or imaging agents, leveraging its indole moiety for optical properties.
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