(S)-3-(4-Fluorobenzyl)Piperidine

95%

Reagent Code: #236270
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CAS Number 275815-80-0

science Other reagents with same CAS 275815-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.26 g/mol
Formula C₁₂H₁₆FN
badge Registry Numbers
MDL Number MFCD09842215
thermostat Physical Properties
Boiling Point 276.6±13.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.044±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structural motif is valuable in creating selective receptor modulators, including those targeting dopamine and serotonin receptors. Commonly employed in the production of investigational compounds for treating neurological disorders such as depression, schizophrenia, and Parkinson’s disease. The stereochemistry enhances binding specificity, improving drug efficacy and reducing off-target effects. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its rigid, substituted piperidine framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,740.00
inventory 250mg
10-20 days ฿45,040.00
inventory 1g
10-20 days ฿90,090.00

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(S)-3-(4-Fluorobenzyl)Piperidine
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structural motif is valuable in creating selective receptor modulators, including those targeting dopamine and serotonin receptors. Commonly employed in the production of investigational compounds for treating neurological disorders such as depression, schizophrenia, and Parkinson’s disease. The stereochemistry enhances binding specificity, improving drug

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structural motif is valuable in creating selective receptor modulators, including those targeting dopamine and serotonin receptors. Commonly employed in the production of investigational compounds for treating neurological disorders such as depression, schizophrenia, and Parkinson’s disease. The stereochemistry enhances binding specificity, improving drug efficacy and reducing off-target effects. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its rigid, substituted piperidine framework.

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