Trans-(1-benzyl-4-(2-fluoro-5-(trifluoromethyl)phenyl)pyrrolidin-3-yl)methanol

98%

Reagent Code: #241909

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 353.36 g/mol
Formula C₁₉H₁₉F₄NO
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its structural features make it valuable for optimizing metabolic stability and receptor binding affinity in drug candidates. Commonly employed in the design of serotonin and dopamine modulators due to its chiral pyrrolidine core and fluorinated aromatic group, which enhance blood-brain barrier penetration. Also utilized in structure-activity relationship (SAR) studies to improve potency and selectivity of neuroactive drugs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,640.00
inventory 1g
10-20 days ฿23,760.00
inventory 100mg
10-20 days ฿5,760.00

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Trans-(1-benzyl-4-(2-fluoro-5-(trifluoromethyl)phenyl)pyrrolidin-3-yl)methanol
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its structural features make it valuable for optimizing metabolic stability and receptor binding affinity in drug candidates. Commonly employed in the design of serotonin and dopamine modulators due to its chiral pyrrolidine core and fluorinated aromatic group, which enhance blood-brain barrier penetration. Also utilized in structure-ac

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its structural features make it valuable for optimizing metabolic stability and receptor binding affinity in drug candidates. Commonly employed in the design of serotonin and dopamine modulators due to its chiral pyrrolidine core and fluorinated aromatic group, which enhance blood-brain barrier penetration. Also utilized in structure-activity relationship (SAR) studies to improve potency and selectivity of neuroactive drugs.

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