(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
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
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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