(4-(4-Methylpiperazin-1-yl)phenyl)methanamine hydrochloride

95%

Reagent Code: #113273
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CAS Number 1810070-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.76 g/mol
Formula C₁₂H₂₀ClN₃
inventory_2 Storage & Handling
Storage room temperature, dry

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 neurological and psychiatric disorders. Its structural features make it suitable for the development of receptor ligands, which can interact with specific proteins in the brain to modulate their activity. Additionally, it is employed in the creation of compounds with potential anticancer properties, as its piperazine moiety can enhance binding affinity to certain cellular targets. Researchers also explore its use in designing drugs for cardiovascular diseases due to its ability to influence specific enzymatic pathways. Its hydrochloride form ensures stability and solubility, making it suitable for laboratory experiments and drug formulation processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿450.00
inventory 1g
10-20 days ฿1,620.00
(4-(4-Methylpiperazin-1-yl)phenyl)methanamine hydrochloride
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 neurological and psychiatric disorders. Its structural features make it suitable for the development of receptor ligands, which can interact with specific proteins in the brain to modulate their activity. Additionally, it is employed in the creation of compounds with potential anticancer properties, as its piperazine moiety can enhance binding affinity to certain cellular targets. Researchers also explore its use in designing drugs for cardiovascular diseases due to its ability to influence specific enzymatic pathways. Its hydrochloride form ensures stability and solubility, making it suitable for laboratory experiments and drug formulation processes.
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