(S)-2-Amino-3-(perfluorophenyl)propanoic acid

95%

Reagent Code: #234922
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CAS Number 34702-59-5

science Other reagents with same CAS 34702-59-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.14 g/mol
Formula C₉H₆F₅NO₂
badge Registry Numbers
MDL Number MFCD01860881
thermostat Physical Properties
Boiling Point 286.3°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and bioactive molecules, particularly where enhanced metabolic stability and lipophilicity are desired. The perfluorophenyl group imparts strong electron-withdrawing properties and improves binding selectivity in peptide-based drugs. It is employed in medicinal chemistry for developing protease inhibitors and receptor ligands, taking advantage of its stereochemical purity to influence biological activity. Also utilized in materials science for designing fluorinated peptides with unique folding and self-assembly behavior.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,000.00
inventory 250mg
10-20 days ฿896.50
inventory 1g
10-20 days ฿2,952.00

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(S)-2-Amino-3-(perfluorophenyl)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals and bioactive molecules, particularly where enhanced metabolic stability and lipophilicity are desired. The perfluorophenyl group imparts strong electron-withdrawing properties and improves binding selectivity in peptide-based drugs. It is employed in medicinal chemistry for developing protease inhibitors and receptor ligands, taking advantage of its stereochemical purity to influence biological activity. Also utilized in materials scien

Used as a chiral building block in the synthesis of pharmaceuticals and bioactive molecules, particularly where enhanced metabolic stability and lipophilicity are desired. The perfluorophenyl group imparts strong electron-withdrawing properties and improves binding selectivity in peptide-based drugs. It is employed in medicinal chemistry for developing protease inhibitors and receptor ligands, taking advantage of its stereochemical purity to influence biological activity. Also utilized in materials science for designing fluorinated peptides with unique folding and self-assembly behavior.

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