tert-Butyl 3-(3-methoxy-3-oxopropanoyl)-piperidine-1-carboxylate

≥95%

Reagent Code: #148682
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CAS Number 891494-65-8

science Other reagents with same CAS 891494-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.34 g/mol
Formula C₁₄H₂₃NO₅
badge Registry Numbers
MDL Number MFCD11974562
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex piperidine-based frameworks, which are common in medicinal chemistry for central nervous system agents, enzyme inhibitors, and receptor modulators. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocycle synthesis, allowing selective reactivity at other functional sites. The ester moiety enables further derivatization, such as hydrolysis or coupling reactions, making it valuable in multi-step organic synthesis for fine chemicals and active pharmaceutical ingredients (APIs).

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Test Parameter Specification
Appearance Yellow Liquid
Purity 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,540.00
inventory 1g
10-20 days ฿11,330.00

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tert-Butyl 3-(3-methoxy-3-oxopropanoyl)-piperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex piperidine-based frameworks, which are common in medicinal chemistry for central nervous system agents, enzyme inhibitors, and receptor modulators. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocycle synthesis, allowing selective reactivity at other functional sites. The ester

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex piperidine-based frameworks, which are common in medicinal chemistry for central nervous system agents, enzyme inhibitors, and receptor modulators. The tert-butyl carbamate (Boc) group provides protection during peptide or heterocycle synthesis, allowing selective reactivity at other functional sites. The ester moiety enables further derivatization, such as hydrolysis or coupling reactions, making it valuable in multi-step organic synthesis for fine chemicals and active pharmaceutical ingredients (APIs).

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