(S)-2-Amino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid

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Reagent Code: #78489
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CAS Number 610794-20-2

science Other reagents with same CAS 610794-20-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.24 g/mol
Formula C₁₂H₁₃NO₃
badge Registry Numbers
MDL Number MFCD21363200
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This compound is primarily explored in the field of medicinal chemistry for its potential as a building block in the synthesis of biologically active molecules. Its structure, featuring an amino acid backbone and a propargyl ether group, makes it a versatile intermediate for developing enzyme inhibitors or receptor modulators. It is particularly useful in designing compounds targeting neurological disorders or inflammation due to its ability to interact with specific biological pathways. Additionally, the alkyne group allows for further functionalization via click chemistry, enabling the creation of complex molecules for drug discovery or biochemical studies. Its applications extend to research in peptide-based therapeutics and as a probe in studying protein interactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,043.00
inventory 1g
10-20 days ฿28,710.00
inventory 100mg
10-20 days ฿7,362.00

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(S)-2-Amino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid
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This compound is primarily explored in the field of medicinal chemistry for its potential as a building block in the synthesis of biologically active molecules. Its structure, featuring an amino acid backbone and a propargyl ether group, makes it a versatile intermediate for developing enzyme inhibitors or receptor modulators. It is particularly useful in designing compounds targeting neurological disorders or inflammation due to its ability to interact with specific biological pathways. Additionally, the alkyne group allows for further functionalization via click chemistry, enabling the creation of complex molecules for drug discovery or biochemical studies. Its applications extend to research in peptide-based therapeutics and as a probe in studying protein interactions.
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