(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-ethylphenyl)propanoic acid

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Reagent Code: #38090
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CAS Number 261380-34-1

science Other reagents with same CAS 261380-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.36 g/mol
Formula C₁₆H₂₃NO₄
badge Registry Numbers
MDL Number MFCD01860633
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the development of biologically active molecules, particularly in the creation of drugs targeting specific receptors or enzymes. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide chemistry, as the Boc group can be selectively removed under mild acidic conditions without affecting other functional groups. Additionally, the presence of the 4-ethylphenyl moiety allows for interactions with hydrophobic regions in target proteins, enhancing its utility in designing compounds with improved binding affinity and selectivity. It is often employed in medicinal chemistry research for the development of potential therapeutics for conditions such as inflammation, cancer, and metabolic disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,368.00
inventory 250mg
10-20 days ฿20,745.00

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(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-ethylphenyl)propanoic acid
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This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the development of biologically active molecules, particularly in the creation of drugs targeting specific receptors or enzymes. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide chemistry, as the Boc group can be selectively removed under mild acidic conditions without affecting other functional groups. Additionally, the pre

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the development of biologically active molecules, particularly in the creation of drugs targeting specific receptors or enzymes. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide chemistry, as the Boc group can be selectively removed under mild acidic conditions without affecting other functional groups. Additionally, the presence of the 4-ethylphenyl moiety allows for interactions with hydrophobic regions in target proteins, enhancing its utility in designing compounds with improved binding affinity and selectivity. It is often employed in medicinal chemistry research for the development of potential therapeutics for conditions such as inflammation, cancer, and metabolic disorders.

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