1-Boc-4-[(N-methoxy-N-methylcarbamoyl)methyl]piperidine

≥97%

Reagent Code: #172290
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CAS Number 416852-69-2

science Other reagents with same CAS 416852-69-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.37 g/mol
Formula C₁₄H₂₆N₂O₄
badge Registry Numbers
MDL Number MFCD07370046
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the preparation of bioactive molecules and drug candidates. Its protected piperidine core allows for selective functionalization, making it valuable in the development of central nervous system agents and receptor modulators. The Boc group enables reversible protection of amines during peptide or heterocycle synthesis, while the methoxy(methyl)carbamoyl side chain can act as a masked carboxylic acid or serve in coupling reactions. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing scaffolds.

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inventory 5g
10-20 days ฿67,780.00

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1-Boc-4-[(N-methoxy-N-methylcarbamoyl)methyl]piperidine
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Used as an intermediate in pharmaceutical synthesis, particularly in the preparation of bioactive molecules and drug candidates. Its protected piperidine core allows for selective functionalization, making it valuable in the development of central nervous system agents and receptor modulators. The Boc group enables reversible protection of amines during peptide or heterocycle synthesis, while the methoxy(methyl)carbamoyl side chain can act as a masked carboxylic acid or serve in coupling reactions. Commonly
Used as an intermediate in pharmaceutical synthesis, particularly in the preparation of bioactive molecules and drug candidates. Its protected piperidine core allows for selective functionalization, making it valuable in the development of central nervous system agents and receptor modulators. The Boc group enables reversible protection of amines during peptide or heterocycle synthesis, while the methoxy(methyl)carbamoyl side chain can act as a masked carboxylic acid or serve in coupling reactions. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing scaffolds.
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