Methyl (S)-2-amino-3-(3-fluoro-4-hydroxyphenyl)propanoate hydrochloride

95%

Reagent Code: #233246
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CAS Number 875574-10-0

science Other reagents with same CAS 875574-10-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.67 g/mol
Formula C₁₀H₁₃ClFNO₃
badge Registry Numbers
MDL Number MFCD24434873
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key chiral building block in organic synthesis, particularly for the preparation of pharmaceutical intermediates and active pharmaceutical ingredients (APIs). The (S)-enantiomer provides stereospecificity essential for biological activity in drug molecules. Its fluorinated aromatic structure with a phenolic hydroxy group enables further derivatization to enhance pharmacokinetic properties and target selectivity. The hydrochloride salt form offers improved solubility, stability, and handling during synthetic processes. Commonly utilized in medicinal chemistry research and development for therapeutics in central nervous system (CNS) disorders, metabolic conditions, and other areas requiring enantiomerically pure compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,050.00
inventory 250mg
10-20 days ฿33,020.00
Methyl (S)-2-amino-3-(3-fluoro-4-hydroxyphenyl)propanoate hydrochloride
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Used as a key chiral building block in organic synthesis, particularly for the preparation of pharmaceutical intermediates and active pharmaceutical ingredients (APIs). The (S)-enantiomer provides stereospecificity essential for biological activity in drug molecules. Its fluorinated aromatic structure with a phenolic hydroxy group enables further derivatization to enhance pharmacokinetic properties and target selectivity. The hydrochloride salt form offers improved solubility, stability, and handling during
Used as a key chiral building block in organic synthesis, particularly for the preparation of pharmaceutical intermediates and active pharmaceutical ingredients (APIs). The (S)-enantiomer provides stereospecificity essential for biological activity in drug molecules. Its fluorinated aromatic structure with a phenolic hydroxy group enables further derivatization to enhance pharmacokinetic properties and target selectivity. The hydrochloride salt form offers improved solubility, stability, and handling during synthetic processes. Commonly utilized in medicinal chemistry research and development for therapeutics in central nervous system (CNS) disorders, metabolic conditions, and other areas requiring enantiomerically pure compounds.
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