(S)-8-Fluorochroman-4-Amine

97%

Reagent Code: #237171
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CAS Number 1003887-62-4

science Other reagents with same CAS 1003887-62-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.18 g/mol
Formula C₉H₁₀FNO
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its fluorinated chroman structure with an amine functional group enables enhanced binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of serotonin and dopamine receptor modulators for treating neurological disorders such as depression, anxiety, and Parkinson’s disease. The (S)-enantiomer’s stereochemistry is critical for biological activity, making it valuable in asymmetric synthesis routes for active pharmaceutical ingredients (APIs).

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,170.00
inventory 250mg
10-20 days ฿19,570.00
inventory 1g
10-20 days ฿64,630.00
(S)-8-Fluorochroman-4-Amine
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its fluorinated chroman structure with an amine functional group enables enhanced binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of serotonin and dopamine receptor modulators for treating neurological disorders such as depression, anxiety, and Parkinson’s disease. The (S)-enantiomer’s stereochemistry is critica

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its fluorinated chroman structure with an amine functional group enables enhanced binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of serotonin and dopamine receptor modulators for treating neurological disorders such as depression, anxiety, and Parkinson’s disease. The (S)-enantiomer’s stereochemistry is critical for biological activity, making it valuable in asymmetric synthesis routes for active pharmaceutical ingredients (APIs).

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