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

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Reagent Code: #231122
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CAS Number 1391539-49-3

science Other reagents with same CAS 1391539-49-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.64 g/mol
Formula C₉H₁₁ClF₃NO
badge Registry Numbers
MDL Number MFCD12758184
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 to neurotransmitter receptors. Commonly employed in the production of antidepressants and anxiolytic drugs due to its ability to influence serotonergic and noradrenergic pathways. The presence of trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. Also utilized in asymmetric synthesis for constructing complex molecules requiring high enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,600.00
inventory 250mg
10-20 days ฿19,710.00
inventory 1g
10-20 days ฿63,610.00

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(R)-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 to neurotransmitter receptors. Commonly employed in the production of antidepressants and anxiolytic drugs due to its ability to influence serotonergic and noradrenergic pathways. The presence of trifluoromethyl group enhances metabolic stability and l

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 to neurotransmitter receptors. Commonly employed in the production of antidepressants and anxiolytic drugs due to its ability to influence serotonergic and noradrenergic pathways. The presence of trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. Also utilized in asymmetric synthesis for constructing complex molecules requiring high enantiomeric purity.

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