3-(1-((Benzyloxy)carbonyl)piperidin-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
≥95%
- Product Code: 41817
CAS:
195877-90-8
| Molecular Weight: | 406.47 g./mol | Molecular Formula: | C₂₁H₃₀N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179070 | |
| Melting Point: | Boiling Point: | 578.5±35.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs and bioactive compounds. The presence of both benzyloxycarbonyl and tert-butoxycarbonyl protecting groups makes it valuable for selective deprotection strategies during the synthesis of complex molecules. It is often employed in the construction of peptides, particularly in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of amino acids. Additionally, its structural features make it suitable for exploring structure-activity relationships (SAR) in drug discovery, particularly for targeting enzymes or receptors involved in various diseases. Its application extends to the preparation of prodrugs and modified peptides with enhanced stability or bioavailability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,707.00 |
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| 0.250 | 10-20 days | ฿9,414.00 |
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3-(1-((Benzyloxy)carbonyl)piperidin-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs and bioactive compounds. The presence of both benzyloxycarbonyl and tert-butoxycarbonyl protecting groups makes it valuable for selective deprotection strategies during the synthesis of complex molecules. It is often employed in the construction of peptides, particularly in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of amino acids. Additionally, its structural features make it suitable for exploring structure-activity relationships (SAR) in drug discovery, particularly for targeting enzymes or receptors involved in various diseases. Its application extends to the preparation of prodrugs and modified peptides with enhanced stability or bioavailability.
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