Ethyl 2-((tert-butoxycarbonyl)amino)-1H-indole-3-carboxylate
95%
- Product Code: 83548
CAS:
1160995-04-9
| Molecular Weight: | 304.34 g./mol | Molecular Formula: | C₁₆H₂₀N₂O₄ |
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| EC Number: | MDL Number: | MFCD11973830 | |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the pharmaceutical and research industries. It serves as a key intermediate in the production of various biologically active compounds, including indole-based molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis and the development of drug candidates. The compound is often employed in the synthesis of complex organic molecules, where the Boc group can be selectively removed under mild conditions, allowing for further functionalization. Additionally, it is utilized in the study of indole derivatives, which are known for their diverse pharmacological properties, such as anti-inflammatory, anticancer, and antimicrobial activities. Its role in facilitating the synthesis of these compounds highlights its importance in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿18,720.00 |
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Ethyl 2-((tert-butoxycarbonyl)amino)-1H-indole-3-carboxylate
This chemical is primarily used in organic synthesis, particularly in the pharmaceutical and research industries. It serves as a key intermediate in the production of various biologically active compounds, including indole-based molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis and the development of drug candidates. The compound is often employed in the synthesis of complex organic molecules, where the Boc group can be selectively removed under mild conditions, allowing for further functionalization. Additionally, it is utilized in the study of indole derivatives, which are known for their diverse pharmacological properties, such as anti-inflammatory, anticancer, and antimicrobial activities. Its role in facilitating the synthesis of these compounds highlights its importance in medicinal chemistry and drug discovery.
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