Methyl (S)-3-amino-3-(3,5-difluorophenyl)propanoate hydrochloride

95%

Reagent Code: #233471
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CAS Number 2703746-08-9

science Other reagents with same CAS 2703746-08-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.66 g/mol
Formula C₁₀H₁₂ClF₂NO₂
badge Registry Numbers
MDL Number MFCD24426234
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the production of pharmaceuticals targeting central nervous system disorders. Its fluorinated aromatic structure and amine functionality make it valuable for developing potent, selective drug candidates, especially in the class of serotonin or dopamine receptor modulators. The compound’s ester group allows for easy further derivatization, enabling efficient incorporation into complex molecules during drug development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,580.00
inventory 250mg
10-20 days ฿30,780.00

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Methyl (S)-3-amino-3-(3,5-difluorophenyl)propanoate hydrochloride
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the production of pharmaceuticals targeting central nervous system disorders. Its fluorinated aromatic structure and amine functionality make it valuable for developing potent, selective drug candidates, especially in the class of serotonin or dopamine receptor modulators. The compound’s ester group allows for easy further derivatization, enabling efficient incorporation into complex molecules during drug

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the production of pharmaceuticals targeting central nervous system disorders. Its fluorinated aromatic structure and amine functionality make it valuable for developing potent, selective drug candidates, especially in the class of serotonin or dopamine receptor modulators. The compound’s ester group allows for easy further derivatization, enabling efficient incorporation into complex molecules during drug development.

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