Methyl (S)-2-amino-3-(3-fluorophenyl)propanoate hydrochloride

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Reagent Code: #203113
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CAS Number 176896-74-5

science Other reagents with same CAS 176896-74-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.67 g/mol
Formula C₁₀H₁₃ClFNO₂
badge Registry Numbers
MDL Number MFCD12911130
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of central nervous system (CNS) active compounds. Its fluorinated phenyl group and chiral center make it valuable for developing drugs with high selectivity and improved metabolic stability. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors, where the stereochemistry plays a critical role in biological activity. The ester functionality allows for easy further derivatization, making it suitable for use in multi-step organic syntheses. Its hydrochloride salt form enhances solubility and handling in aqueous and polar environments during drug development processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿5,310.00
inventory 5g
10-20 days ฿18,430.00

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Methyl (S)-2-amino-3-(3-fluorophenyl)propanoate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of central nervous system (CNS) active compounds. Its fluorinated phenyl group and chiral center make it valuable for developing drugs with high selectivity and improved metabolic stability. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors, where the stereochemistry plays a critical role in biological activity. The ester functionality allows for easy further

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of central nervous system (CNS) active compounds. Its fluorinated phenyl group and chiral center make it valuable for developing drugs with high selectivity and improved metabolic stability. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors, where the stereochemistry plays a critical role in biological activity. The ester functionality allows for easy further derivatization, making it suitable for use in multi-step organic syntheses. Its hydrochloride salt form enhances solubility and handling in aqueous and polar environments during drug development processes.

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