3-Methyl-2-(1-piperazinyl)quinoline

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Reagent Code: #214377
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CAS Number 348133-74-4

science Other reagents with same CAS 348133-74-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.31 g/mol
Formula C₁₄H₁₇N₃
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MDL Number MFCD08061017
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. Shows potential in the development of central nervous system agents due to its structural affinity with neuroactive molecules. Investigated for its role in modulating receptor activity, particularly in psychiatric and neurological drug discovery. Also employed in the preparation of fluorescent probes for biochemical assays owing to its quinoline backbone, which exhibits favorable photophysical properties. Its piperazinyl group enhances solubility and binding selectivity, making it suitable for optimizing drug candidates in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,790.00

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3-Methyl-2-(1-piperazinyl)quinoline
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Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. Shows potential in the development of central nervous system agents due to its structural affinity with neuroactive molecules. Investigated for its role in modulating receptor activity, particularly in psychiatric and neurological drug discovery. Also employed in the preparation of fluorescent probes for biochemical assays owing to its quinoline backbone, which exhibits favorable photophysical

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. Shows potential in the development of central nervous system agents due to its structural affinity with neuroactive molecules. Investigated for its role in modulating receptor activity, particularly in psychiatric and neurological drug discovery. Also employed in the preparation of fluorescent probes for biochemical assays owing to its quinoline backbone, which exhibits favorable photophysical properties. Its piperazinyl group enhances solubility and binding selectivity, making it suitable for optimizing drug candidates in medicinal chemistry.

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