(5-Nitro-pyridin-2-yl)-piperidin-3-yl-amine

97%

Reagent Code: #219542
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CAS Number 916791-13-4

science Other reagents with same CAS 916791-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.244 g/mol
Formula C₁₀H₁₄N₄O₂
badge Registry Numbers
MDL Number MFCD08752671
inventory_2 Storage & Handling
Density 1.288 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Commonly employed in research settings to design compounds with improved metabolic stability and bioavailability. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,610.00
inventory 500mg
10-20 days ฿16,140.00
(5-Nitro-pyridin-2-yl)-piperidin-3-yl-amine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Commonly employed in research settings to design compounds with improved metabolic stability and bioavailability. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric pr

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Commonly employed in research settings to design compounds with improved metabolic stability and bioavailability. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates.

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