4-(1-Piperazinyl)-2-(trifluoromethyl)quinoline

≥95%

Reagent Code: #228293
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CAS Number 175203-79-9

science Other reagents with same CAS 175203-79-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.28 g/mol
Formula C₁₄H₁₄F₃N₃
badge Registry Numbers
MDL Number MFCD00219765
thermostat Physical Properties
Melting Point 133-135 °C
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in pharmaceutical research as a key intermediate for synthesizing bioactive compounds, particularly in the development of antipsychotic and antidepressant drugs. Its structure supports binding to central nervous system receptors, making it valuable in medicinal chemistry for designing novel therapeutics. Also employed in the synthesis of kinase inhibitors and other targeted agents in oncology research. Shows potential in improving metabolic stability and blood-brain barrier penetration in drug candidates due to the trifluoromethyl and quinoline moieties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿22,200.00
4-(1-Piperazinyl)-2-(trifluoromethyl)quinoline
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Used in pharmaceutical research as a key intermediate for synthesizing bioactive compounds, particularly in the development of antipsychotic and antidepressant drugs. Its structure supports binding to central nervous system receptors, making it valuable in medicinal chemistry for designing novel therapeutics. Also employed in the synthesis of kinase inhibitors and other targeted agents in oncology research. Shows potential in improving metabolic stability and blood-brain barrier penetration in drug candi

Used in pharmaceutical research as a key intermediate for synthesizing bioactive compounds, particularly in the development of antipsychotic and antidepressant drugs. Its structure supports binding to central nervous system receptors, making it valuable in medicinal chemistry for designing novel therapeutics. Also employed in the synthesis of kinase inhibitors and other targeted agents in oncology research. Shows potential in improving metabolic stability and blood-brain barrier penetration in drug candidates due to the trifluoromethyl and quinoline moieties.

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