Tert-Butyl 2-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate

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Reagent Code: #238246
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CAS Number 211310-10-0

science Other reagents with same CAS 211310-10-0

blur_circular Chemical Specifications

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Weight 272.34 g/mol
Formula C₁₃H₂₄N₂O₄
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex piperidine-based compounds, which are common in central nervous system agents, receptor modulators, and enzyme inhibitors. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocyclic synthesis, allowing selective reactivity at other functional sites. The methoxy(methyl)carbamoyl moiety can act as a masked amine or be tailored for specific metabolic stability and binding affinity in final active ingredients. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,270.00

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Tert-Butyl 2-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex piperidine-based compounds, which are common in central nervous system agents, receptor modulators, and enzyme inhibitors. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocyclic synthesis, allowing selective reactivity at other functional sites. The methoxy(methyl)carbamoyl moiety can act as a m

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex piperidine-based compounds, which are common in central nervous system agents, receptor modulators, and enzyme inhibitors. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocyclic synthesis, allowing selective reactivity at other functional sites. The methoxy(methyl)carbamoyl moiety can act as a masked amine or be tailored for specific metabolic stability and binding affinity in final active ingredients. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies.

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