1-Boc-1,2,5,6-tetrahydropyridine-3-carboxylic acid

98%

Reagent Code: #146237
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CAS Number 86447-11-2

science Other reagents with same CAS 86447-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.26 g/mol
Formula C₁₁H₁₇NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require substituted piperidine or tetrahydropyridine moieties. Its protected amine group allows for selective reactions at other functional sites, making it valuable in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles found in bioactive molecules. The Boc-protected structure enhances stability and solubility during peptide coupling and other condensation reactions. Widely applied in research settings for drug discovery, especially in central nervous system agents and kinase inhibitors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿2,800.00

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1-Boc-1,2,5,6-tetrahydropyridine-3-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require substituted piperidine or tetrahydropyridine moieties. Its protected amine group allows for selective reactions at other functional sites, making it valuable in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles found in bioactive molecules. The Boc-protected structure enhance

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require substituted piperidine or tetrahydropyridine moieties. Its protected amine group allows for selective reactions at other functional sites, making it valuable in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles found in bioactive molecules. The Boc-protected structure enhances stability and solubility during peptide coupling and other condensation reactions. Widely applied in research settings for drug discovery, especially in central nervous system agents and kinase inhibitors.

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