1-(4-Trifluoromethylphenyl)piperidine-4-carboxylic acid

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Reagent Code: #240835
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CAS Number 607354-69-8

science Other reagents with same CAS 607354-69-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.25 g/mol
Formula C₁₃H₁₄F₃NO₂
badge Registry Numbers
MDL Number MFCD05864757
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the design of ligands targeting dopamine and sigma receptors, making it valuable in research for antipsychotic and neurodegenerative disease treatments. The trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. It is also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿770.00
inventory 1g
10-20 days ฿2,550.00
inventory 10g
10-20 days ฿22,230.00
inventory 5g
10-20 days ฿11,120.00

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1-(4-Trifluoromethylphenyl)piperidine-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the design of ligands targeting dopamine and sigma receptors, making it valuable in research for antipsychotic and neurodegenerative disease treatments. The trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. It is also employed in medicinal chemistry for structure-activit

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the design of ligands targeting dopamine and sigma receptors, making it valuable in research for antipsychotic and neurodegenerative disease treatments. The trifluoromethyl group enhances metabolic stability and lipophilicity, improving blood-brain barrier penetration. It is also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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