2-((2-(Piperidin-1-yl)pyrimidin-4-yl)amino)benzoic acid

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Reagent Code: #132146
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CAS Number 324778-48-5

science Other reagents with same CAS 324778-48-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.34 g/mol
Formula C₁₆H₁₈N₄O₂
thermostat Physical Properties
Boiling Point 537.2±56.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.315±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell signaling. Shows potential in developing treatments for oncological diseases due to its ability to modulate cellular pathways related to proliferation and apoptosis. Also employed in the design of small-molecule therapeutics with improved selectivity and binding affinity. Its structure supports derivatization for optimizing pharmacokinetic properties in drug development programs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿17,890.00
inventory 50mg
10-20 days ฿30,390.00
inventory 100mg
10-20 days ฿51,640.00

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2-((2-(Piperidin-1-yl)pyrimidin-4-yl)amino)benzoic acid
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell signaling. Shows potential in developing treatments for oncological diseases due to its ability to modulate cellular pathways related to proliferation and apoptosis. Also employed in the design of small-molecule therapeutics with improved selectivity and binding affinity. Its structure supports derivatization for optimizing pharmacokinetic proper

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell signaling. Shows potential in developing treatments for oncological diseases due to its ability to modulate cellular pathways related to proliferation and apoptosis. Also employed in the design of small-molecule therapeutics with improved selectivity and binding affinity. Its structure supports derivatization for optimizing pharmacokinetic properties in drug development programs.

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