Bis(4-methyl-2-(piperidin-1-yl)quinolin-6-yl)methane trihydrochloride

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Reagent Code: #60640
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CAS Number 5463-36-5

science Other reagents with same CAS 5463-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.5508 g/mol
Formula C₂₂H₃₁NO₄S
badge Registry Numbers
MDL Number MFCD28016467
thermostat Physical Properties
Boiling Point 569.5 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.246 g/cm3
Storage room temperature, inert gas

description Product Description

This compound is primarily utilized in research and development within the field of medicinal chemistry. It serves as a key intermediate or building block in the synthesis of more complex molecules, particularly those targeting biological pathways. Its structure suggests potential applications in the development of pharmaceuticals, especially in areas such as oncology or neurology, where quinoline derivatives are often explored for their therapeutic properties. Additionally, it may be used in biochemical studies to investigate interactions with specific receptors or enzymes, aiding in the discovery of novel drug candidates. Its trihydrochloride form enhances solubility, making it suitable for experimental use in aqueous environments.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿84,987.00
inventory 250mg
10-20 days ฿31,320.00

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Bis(4-methyl-2-(piperidin-1-yl)quinolin-6-yl)methane trihydrochloride
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This compound is primarily utilized in research and development within the field of medicinal chemistry. It serves as a key intermediate or building block in the synthesis of more complex molecules, particularly those targeting biological pathways. Its structure suggests potential applications in the development of pharmaceuticals, especially in areas such as oncology or neurology, where quinoline derivatives are often explored for their therapeutic properties. Additionally, it may be used in biochemical studies to investigate interactions with specific receptors or enzymes, aiding in the discovery of novel drug candidates. Its trihydrochloride form enhances solubility, making it suitable for experimental use in aqueous environments.
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