2-((tert-Butoxycarbonyl)amino)-3-(3-chlorophenyl)propanoic acid

95%

Reagent Code: #150922
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CAS Number 188814-25-7

science Other reagents with same CAS 188814-25-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.75 g/mol
Formula C₁₄H₁₈ClNO₄
badge Registry Numbers
MDL Number MFCD06656168
thermostat Physical Properties
Boiling Point 452.5±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.245±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports peptide mimetic design, making it valuable in medicinal chemistry for creating analogs with enhanced stability and binding affinity. Commonly employed in solid-phase and solution-phase peptide synthesis where protection of the amine group is required. The chlorophenyl moiety can influence target selectivity in drug candidates, especially in central nervous system agents and enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,130.00
inventory 250mg
10-20 days ฿13,370.00
inventory 1g
10-20 days ฿18,630.00

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2-((tert-Butoxycarbonyl)amino)-3-(3-chlorophenyl)propanoic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports peptide mimetic design, making it valuable in medicinal chemistry for creating analogs with enhanced stability and binding affinity. Commonly employed in solid-phase and solution-phase peptide synthesis where protection of the amine group is required. The chlorophenyl moiety can influence target selectivity in drug can

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports peptide mimetic design, making it valuable in medicinal chemistry for creating analogs with enhanced stability and binding affinity. Commonly employed in solid-phase and solution-phase peptide synthesis where protection of the amine group is required. The chlorophenyl moiety can influence target selectivity in drug candidates, especially in central nervous system agents and enzyme inhibitors.

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