(S)-2-((tert-butoxycarbonyl)amino)-3-(quinolin-2-yl)propanoic acid
95%
- Product Code: 104354
CAS:
161453-37-8
Molecular Weight: | 316.35 g./mol | Molecular Formula: | C₁₇H₂₀N₂O₄ |
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EC Number: | MDL Number: | MFCD00671380 | |
Melting Point: | Boiling Point: | 505.6±45.0 °C(Predicted) | |
Density: | 1.235±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety, makes it valuable for designing compounds with potential anticancer, antimicrobial, or anti-inflammatory properties. 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 complex molecule assembly. Its application extends to research focused on developing novel therapeutic agents and studying structure-activity relationships in drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $438.52 |
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0.250 | 10-20 days | $655.90 |
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(S)-2-((tert-butoxycarbonyl)amino)-3-(quinolin-2-yl)propanoic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety, makes it valuable for designing compounds with potential anticancer, antimicrobial, or anti-inflammatory properties. 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 complex molecule assembly. Its application extends to research focused on developing novel therapeutic agents and studying structure-activity relationships in drug discovery.
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