((3S,4R)-4-(4-Fluorophenyl)piperidin-3-yl)methanol

95%

Reagent Code: #234941
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CAS Number 125224-43-3

science Other reagents with same CAS 125224-43-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.26 g/mol
Formula C₁₂H₁₆FNO
thermostat Physical Properties
Boiling Point 327.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical agents, particularly as an intermediate in the development of central nervous system (CNS) active compounds. Its structure supports modification for receptor targeting, especially in serotonin and dopamine pathways. Commonly utilized in research for antidepressants, antipsychotics, and analgesic drugs due to its chiral piperidine core and functionalized aromatic ring. The hydroxyl group allows for esterification or ether formation to improve pharmacokinetic properties. Also explored in medicinal chemistry for improving blood-brain barrier penetration in neuroactive molecules.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,100.00
inventory 250mg
10-20 days ฿9,350.00

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((3S,4R)-4-(4-Fluorophenyl)piperidin-3-yl)methanol
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Used in the synthesis of pharmaceutical agents, particularly as an intermediate in the development of central nervous system (CNS) active compounds. Its structure supports modification for receptor targeting, especially in serotonin and dopamine pathways. Commonly utilized in research for antidepressants, antipsychotics, and analgesic drugs due to its chiral piperidine core and functionalized aromatic ring. The hydroxyl group allows for esterification or ether formation to improve pharmacokinetic propert

Used in the synthesis of pharmaceutical agents, particularly as an intermediate in the development of central nervous system (CNS) active compounds. Its structure supports modification for receptor targeting, especially in serotonin and dopamine pathways. Commonly utilized in research for antidepressants, antipsychotics, and analgesic drugs due to its chiral piperidine core and functionalized aromatic ring. The hydroxyl group allows for esterification or ether formation to improve pharmacokinetic properties. Also explored in medicinal chemistry for improving blood-brain barrier penetration in neuroactive molecules.

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