(S)-3-(4-(Allyloxy)phenyl)-2-aminopropanoic acid

98%

Reagent Code: #232498
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CAS Number 107903-42-4

science Other reagents with same CAS 107903-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.25 g/mol
Formula C₁₂H₁₅NO₃
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MDL Number MFCD29077389
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other biologically active molecules. Its chiral amino acid structure makes it valuable in asymmetric synthesis for creating enantioselective drugs. Commonly employed in research settings for designing peptide mimetics and enzyme inhibitors, especially in treatments targeting viral infections and metabolic disorders. Also serves as a building block in medicinal chemistry for optimizing drug potency and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,090.00
inventory 5g
10-20 days ฿28,280.00
(S)-3-(4-(Allyloxy)phenyl)-2-aminopropanoic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other biologically active molecules. Its chiral amino acid structure makes it valuable in asymmetric synthesis for creating enantioselective drugs. Commonly employed in research settings for designing peptide mimetics and enzyme inhibitors, especially in treatments targeting viral infections and metabolic disorders. Also serves as a building block in medicinal chemistry for optimizing drug po

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other biologically active molecules. Its chiral amino acid structure makes it valuable in asymmetric synthesis for creating enantioselective drugs. Commonly employed in research settings for designing peptide mimetics and enzyme inhibitors, especially in treatments targeting viral infections and metabolic disorders. Also serves as a building block in medicinal chemistry for optimizing drug potency and selectivity.

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