1-Boc-piperidine-3-carboxaldehyde

97%

Reagent Code: #143498
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CAS Number 118156-93-7

science Other reagents with same CAS 118156-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.28 g/mol
Formula C₁₁H₁₉NO₃
badge Registry Numbers
MDL Number MFCD02179020
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 active pharmaceutical ingredients (APIs) that require functionalized piperidine scaffolds. Its aldehyde group allows for further chemical transformations such as reductive amination or nucleophilic addition, enabling the construction of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for drug discovery programs, especially in the design of central nervous system (CNS) agents, kinase inhibitors, and bioactive molecules where a substituted piperidine ring enhances pharmacokinetic properties. The Boc-protected amine ensures selective reactivity and stability during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like compound assembly.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿180.00
1g
10-20 days ฿310.00
25g
10-20 days ฿4,680.00
100g
10-20 days ฿16,020.00
5g
10-20 days ฿1,170.00
1-Boc-piperidine-3-carboxaldehyde
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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 aldehyde group allows for further chemical transformations such as reductive amination or nucleophilic addition, enabling the construction of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for drug discovery programs, especially in the design of central nervous system (CNS) agents, kinase inhibitors, and bioactive molecules where a substituted piperidine ring enhances pharmacokinetic properties. The Boc-protected amine ensures selective reactivity and stability during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like compound assembly.
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