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

97%

Reagent Code: #234988
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CAS Number 76757-91-0

science Other reagents with same CAS 76757-91-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.36 g/mol
Formula C₁₆H₂₃NO₅
badge Registry Numbers
MDL Number MFCD00065601
thermostat Physical Properties
Boiling Point 472.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, 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 drugs with improved metabolic stability and target specificity. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc-protecting group, which allows for controlled deprotection and coupling. Also utilized in the preparation of enzyme inhibitors where the 4-ethoxyphenyl moiety contributes to binding affinity and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿410.00
inventory 5g
10-20 days ฿1,770.00
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-ethoxyphenyl)propanoic acid
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Used as a chiral intermediate in the synthesis of pharmaceuticals, 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 drugs with improved metabolic stability and target specificity. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc-protecting group, which allows for controlled deprotection and coupling. Also u

Used as a chiral intermediate in the synthesis of pharmaceuticals, 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 drugs with improved metabolic stability and target specificity. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc-protecting group, which allows for controlled deprotection and coupling. Also utilized in the preparation of enzyme inhibitors where the 4-ethoxyphenyl moiety contributes to binding affinity and selectivity.

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