3-(Methylamino)piperidine dihydrochloride

95%

Reagent Code: #205310
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CAS Number 127294-77-3

science Other reagents with same CAS 127294-77-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.11 g/mol
Formula C₆H₁₄N₂·₂HCl
badge Registry Numbers
MDL Number MFCD00673143
thermostat Physical Properties
Melting Point 199-200°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It serves as a building block for drugs targeting neurological disorders such as depression, anxiety, and psychosis due to its structural similarity to bioactive piperidines. Its methylamino group allows for easy modification, enabling the creation of various derivatives with tailored pharmacological properties. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies. Also utilized in the production of selective receptor ligands, including those acting on serotonin, dopamine, and sigma receptors.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿490.00
3-(Methylamino)piperidine dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It serves as a building block for drugs targeting neurological disorders such as depression, anxiety, and psychosis due to its structural similarity to bioactive piperidines. Its methylamino group allows for easy modification, enabling the creation of various derivatives with tailored pharmacological properties. Commonly employed in medicinal chemistry for structure-acti

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It serves as a building block for drugs targeting neurological disorders such as depression, anxiety, and psychosis due to its structural similarity to bioactive piperidines. Its methylamino group allows for easy modification, enabling the creation of various derivatives with tailored pharmacological properties. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies. Also utilized in the production of selective receptor ligands, including those acting on serotonin, dopamine, and sigma receptors.

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