2-((tert-Butoxycarbonyl)amino)-3-(naphthalen-2-yl)propanoic acid
97%
- Product Code: 58248
CAS:
56583-58-5
Molecular Weight: | 315.36 g./mol | Molecular Formula: | C₁₈H₂₁NO₄ |
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EC Number: | MDL Number: | MFCD01883037 | |
Melting Point: | Boiling Point: | 512.2 °C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where the Boc group is used to protect amino groups during the formation of peptide bonds. The naphthalene moiety in its structure can enhance the binding affinity of peptides to specific biological targets, making it useful in designing inhibitors or modulators for proteins and enzymes. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its application extends to the synthesis of complex organic molecules for use in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,147.00 |
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0.250 | 10-20 days | ฿9,450.00 |
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1.000 | 10-20 days | ฿29,583.00 |
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2-((tert-Butoxycarbonyl)amino)-3-(naphthalen-2-yl)propanoic acid
This compound is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where the Boc group is used to protect amino groups during the formation of peptide bonds. The naphthalene moiety in its structure can enhance the binding affinity of peptides to specific biological targets, making it useful in designing inhibitors or modulators for proteins and enzymes. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its application extends to the synthesis of complex organic molecules for use in medicinal chemistry and drug discovery.
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