4-(4-Benzylpiperazin-1-ylmethyl)phenylamine

98%

Reagent Code: #72267
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CAS Number 422517-70-2

science Other reagents with same CAS 422517-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.4 g/mol
Formula C₁₈H₂₃N₃
thermostat Physical Properties
Boiling Point 429.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting the central nervous system. Its structure, which includes a benzylpiperazine moiety, makes it a valuable building block for developing compounds with potential antipsychotic, antidepressant, or anxiolytic properties. Researchers often explore its derivatives for their affinity to specific receptors, such as serotonin or dopamine receptors, which are critical in treating neurological and psychiatric disorders. Additionally, its amine functionality allows for further chemical modifications, enabling the creation of diverse drug candidates with optimized pharmacokinetic and pharmacodynamic profiles.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,680.00
inventory 1g
10-20 days ฿6,460.00

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4-(4-Benzylpiperazin-1-ylmethyl)phenylamine
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting the central nervous system. Its structure, which includes a benzylpiperazine moiety, makes it a valuable building block for developing compounds with potential antipsychotic, antidepressant, or anxiolytic properties. Researchers often explore its derivatives for their affinity to specific receptors, such as serotonin or dopamine receptors, which are critical in treating neurological and psychiatric disorders. Additionally, its amine functionality allows for further chemical modifications, enabling the creation of diverse drug candidates with optimized pharmacokinetic and pharmacodynamic profiles.
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