(S)-2-Amino-2-(2-(trifluoromethyl)phenyl)ethan-1-ol hydrochloride

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Reagent Code: #236538
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CAS Number 1391449-79-8

science Other reagents with same CAS 1391449-79-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.64 g/mol
Formula C₉H₁₁ClF₃NO
badge Registry Numbers
MDL Number MFCD12758183
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of agents with enhanced selectivity and binding affinity due to the presence of both amino and hydroxyl functional groups in a stereochemically defined arrangement. Commonly employed in the production of antidepressants and anxiolytic drugs, where the (S)-configuration plays a critical role in pharmacological activity. The trifluoromethylphenyl moiety enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. Also utilized in asymmetric synthesis and catalysis research due to its rigid backbone and stereogenic center.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,250.00
inventory 250mg
10-20 days ฿24,640.00
inventory 1g
10-20 days ฿79,510.00

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(S)-2-Amino-2-(2-(trifluoromethyl)phenyl)ethan-1-ol hydrochloride
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of agents with enhanced selectivity and binding affinity due to the presence of both amino and hydroxyl functional groups in a stereochemically defined arrangement. Commonly employed in the production of antidepressants and anxiolytic drugs, where the (S)-configuration plays a critical role in pharmacological a
Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of agents with enhanced selectivity and binding affinity due to the presence of both amino and hydroxyl functional groups in a stereochemically defined arrangement. Commonly employed in the production of antidepressants and anxiolytic drugs, where the (S)-configuration plays a critical role in pharmacological activity. The trifluoromethylphenyl moiety enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. Also utilized in asymmetric synthesis and catalysis research due to its rigid backbone and stereogenic center.
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