3-N-BOC-3-N-METHYL-AMINOMETHYL PIPERIDINE

97%

Reagent Code: #216842
label
Alias tert-butyl N-methyl-N-[(piperidin-3-yl)methyl]carbamate; 3-N-BOC-3-N-methylaminomethylpiperidine
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CAS Number 169750-76-9

science Other reagents with same CAS 169750-76-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.335 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD06800386
thermostat Physical Properties
Boiling Point 306.0±11.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in creating potent bioactive molecules. Commonly employed in the production of central nervous system agents, including certain antidepressants and neuroleptics, due to the structural compatibility of the methylaminomethyl piperidine moiety with neurological targets. Also utilized in medicinal chemistry for building blocks in drug discovery programs, especially in the design of receptor agonists and antagonists.

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inventory 1g
10-20 days ฿8,950.00

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3-N-BOC-3-N-METHYL-AMINOMETHYL PIPERIDINE
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in creating potent bioactive molecules. Commonly employed in the production of central nervous system agents, including certain antidepressants and neuroleptics, due to the structural compatibility of the methylaminomethyl piperidine moiety with neurological targets. Also utilized in medicinal chemistry for building blocks in drug discovery programs, especially in the design of receptor agonists and antagonists.
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