(S)-3-Amino-3-(4-chlorophenyl)propanoic acid

95%

Reagent Code: #234948
label
Alias L-3-amino-3-(4-chlorophenyl)propionic acid; (S)-p-chloro-B-phenylalanine; (S)-p-chloro-B-phenylalanine; H-β-Phe(4-Cl)-OH
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CAS Number 131690-60-3

science Other reagents with same CAS 131690-60-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.63 g/mol
Formula C₉H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD03840457
thermostat Physical Properties
Boiling Point 345.8°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structural motif is valuable in creating gamma-aminobutyric acid (GABA) analogs, which are explored for anticonvulsant, anxiolytic, and analgesic properties. The compound's stereochemistry enhances binding selectivity to neurotransmitter receptors, making it useful in designing drugs with improved efficacy and reduced side effects. It is also employed in medicinal chemistry research for structure-activity relationship (SAR) studies of amino acid derivatives targeting neurological disorders.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,980.00
inventory 1g
10-20 days ฿4,320.00
inventory 5g
10-20 days ฿16,460.00

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(S)-3-Amino-3-(4-chlorophenyl)propanoic acid
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structural motif is valuable in creating gamma-aminobutyric acid (GABA) analogs, which are explored for anticonvulsant, anxiolytic, and analgesic properties. The compound's stereochemistry enhances binding selectivity to neurotransmitter receptors, making it useful in designing drugs with improved efficacy and reduced side effects. It is also employed in

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structural motif is valuable in creating gamma-aminobutyric acid (GABA) analogs, which are explored for anticonvulsant, anxiolytic, and analgesic properties. The compound's stereochemistry enhances binding selectivity to neurotransmitter receptors, making it useful in designing drugs with improved efficacy and reduced side effects. It is also employed in medicinal chemistry research for structure-activity relationship (SAR) studies of amino acid derivatives targeting neurological disorders.

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