(S)-2-((tert-butoxycarbonyl)amino)-3-(quinolin-2-yl)propanoic acid

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Reagent Code: #104354
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CAS Number 161453-37-8

science Other reagents with same CAS 161453-37-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.35 g/mol
Formula C₁₇H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD00671380
thermostat Physical Properties
Boiling Point 505.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.235±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,616.00
inventory 250mg
10-20 days ฿21,861.00

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(S)-2-((tert-butoxycarbonyl)amino)-3-(quinolin-2-yl)propanoic acid
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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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