(S)-2-Methoxy-1-(4-(trifluoromethyl)phenyl)ethan-1-amine hydrochloride

98%

Reagent Code: #233389
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CAS Number 2703746-31-8

science Other reagents with same CAS 2703746-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.66 g/mol
Formula C₁₀H₁₃ClF₃NO
badge Registry Numbers
MDL Number MFCD32852144
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

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, featuring a 2-methoxyethyl chain and a 4-(trifluoromethyl)phenyl moiety, supports the development of selective serotonin reuptake inhibitors (SSRIs) and other neuromodulatory agents. The presence of a trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. Widely employed in asymmetric synthesis due to the chiral amine functionality, enabling the production of enantiomerically pure drugs. Also utilized in the preparation of radiolabeled derivatives for receptor binding studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿36,180.00
(S)-2-Methoxy-1-(4-(trifluoromethyl)phenyl)ethan-1-amine 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, featuring a 2-methoxyethyl chain and a 4-(trifluoromethyl)phenyl moiety, supports the development of selective serotonin reuptake inhibitors (SSRIs) and other neuromodulatory agents. The presence of a trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. Widely employed in

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure, featuring a 2-methoxyethyl chain and a 4-(trifluoromethyl)phenyl moiety, supports the development of selective serotonin reuptake inhibitors (SSRIs) and other neuromodulatory agents. The presence of a trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. Widely employed in asymmetric synthesis due to the chiral amine functionality, enabling the production of enantiomerically pure drugs. Also utilized in the preparation of radiolabeled derivatives for receptor binding studies.

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