(S)-2-((Tert-butoxycarbonyl)amino)-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid
95%
- Product Code: 57122
CAS:
146610-21-1
| Molecular Weight: | 305.33 g./mol | Molecular Formula: | C₁₅H₁₉N₃O₄ |
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| EC Number: | MDL Number: | MFCD08273059 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It serves as a building block for the development of small molecule inhibitors, particularly those targeting protein-protein interactions or enzymes involved in disease pathways. Its structure, featuring a pyrrolopyridine moiety, makes it valuable in designing compounds with potential therapeutic applications, such as anticancer or anti-inflammatory agents. Additionally, it is often employed in peptide synthesis, where the tert-butoxycarbonyl (Boc) group acts as a protective group for the amino functionality, ensuring selective reactions during the construction of complex peptide chains. Its role in drug discovery and development highlights its importance in creating novel pharmaceutical candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,344.00 |
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| 0.250 | 10-20 days | ฿11,016.00 |
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| 1.000 | 10-20 days | ฿27,531.00 |
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(S)-2-((Tert-butoxycarbonyl)amino)-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It serves as a building block for the development of small molecule inhibitors, particularly those targeting protein-protein interactions or enzymes involved in disease pathways. Its structure, featuring a pyrrolopyridine moiety, makes it valuable in designing compounds with potential therapeutic applications, such as anticancer or anti-inflammatory agents. Additionally, it is often employed in peptide synthesis, where the tert-butoxycarbonyl (Boc) group acts as a protective group for the amino functionality, ensuring selective reactions during the construction of complex peptide chains. Its role in drug discovery and development highlights its importance in creating novel pharmaceutical candidates.
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