(S)-Ethyl 3-(4-(benzyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoate

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Reagent Code: #38401
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CAS Number 127132-32-5

science Other reagents with same CAS 127132-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 399.48 g/mol
Formula C₂₃H₂₉NO₅
badge Registry Numbers
MDL Number MFCD26407317
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the production of biologically active compounds, including peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where selective protection and deprotection of functional groups are essential. Additionally, the benzyloxy group enhances its solubility and reactivity in organic reactions, facilitating its use in medicinal chemistry for designing potential therapeutic agents. Its application is also observed in the study of enzyme inhibitors and receptor modulators, contributing to advancements in drug discovery.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,185.00
inventory 250mg
10-20 days ฿450.00
inventory 1g
10-20 days ฿1,197.00

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(S)-Ethyl 3-(4-(benzyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoate
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the production of biologically active compounds, including peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where selective protection and deprotection of functional groups are essential. Additionally, the benzyloxy group enhances its solubility and reactivity in organic reactions, facilitating its use in medicinal chemistry for designing potential therapeutic agents. Its application is also observed in the study of enzyme inhibitors and receptor modulators, contributing to advancements in drug discovery.
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