(R)-3-((tert-Butoxycarbonyl)amino)-4-(p-tolyl)butanoic acid
98%
- Product Code: 104259
CAS:
269398-85-8
Molecular Weight: | 293.36 g./mol | Molecular Formula: | C₁₆H₂₃NO₄ |
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EC Number: | MDL Number: | MFCD01860928 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of peptide-based drugs. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways, such as enzyme inhibition or receptor modulation. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide coupling reactions, ensuring selective and efficient synthesis. Additionally, it is employed in research laboratories for the preparation of chiral molecules, contributing to the study of stereochemistry in drug design. Its applications are critical in advancing medicinal chemistry and the creation of therapeutic agents.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿4,248.00 |
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0.250 | 10-20 days | ฿6,318.00 |
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1.000 | 10-20 days | ฿15,804.00 |
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(R)-3-((tert-Butoxycarbonyl)amino)-4-(p-tolyl)butanoic acid
This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of peptide-based drugs. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways, such as enzyme inhibition or receptor modulation. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide coupling reactions, ensuring selective and efficient synthesis. Additionally, it is employed in research laboratories for the preparation of chiral molecules, contributing to the study of stereochemistry in drug design. Its applications are critical in advancing medicinal chemistry and the creation of therapeutic agents.
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