5-Nitro-2-(piperidin-1-yl)pyridine

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Reagent Code: #219679
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CAS Number 26820-61-1

science Other reagents with same CAS 26820-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.229 g/mol
Formula C₁₀H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD00086192
thermostat Physical Properties
Melting Point 83-84 °C
Boiling Point 380.4 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.242 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocyclic systems, which are common in drug design. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity and selectivity toward specific enzyme targets. Also utilized in research settings for the preparation of novel analogs in structure-activity relationship (SAR) studies.

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inventory 1g
10-20 days ฿18,660.00

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5-Nitro-2-(piperidin-1-yl)pyridine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocyclic systems, which are common in drug design. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity and selectivity toward specific enzyme targets. Also utilized in research settings for the preparation of novel analogs in structure

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocyclic systems, which are common in drug design. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance binding affinity and selectivity toward specific enzyme targets. Also utilized in research settings for the preparation of novel analogs in structure-activity relationship (SAR) studies.

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