N-(3-Chloro-4-((5-chloropyridin-2-yl)oxy)phenyl)picolinamide

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Reagent Code: #215688
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CAS Number 1630936-95-6

science Other reagents with same CAS 1630936-95-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 360.19 g/mol
Formula C₁₇H₁₁Cl₂N₃O₂
badge Registry Numbers
MDL Number MFCD28411626
thermostat Physical Properties
Melting Point 154-158 °C
Boiling Point 422.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.445±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as an intermediate in the synthesis of tyrosine kinase inhibitors, particularly in the development of anticancer agents. It plays a key role in targeting epidermal growth factor receptor (EGFR) pathways, which are involved in tumor cell proliferation and survival. Commonly applied in pharmaceutical research for lung, breast, and other solid tumor treatments. Also utilized in structure-activity relationship (SAR) studies to optimize inhibitor potency and selectivity.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿13,500.00
inventory 50mg
10-20 days ฿56,250.00

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N-(3-Chloro-4-((5-chloropyridin-2-yl)oxy)phenyl)picolinamide
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Used as an intermediate in the synthesis of tyrosine kinase inhibitors, particularly in the development of anticancer agents. It plays a key role in targeting epidermal growth factor receptor (EGFR) pathways, which are involved in tumor cell proliferation and survival. Commonly applied in pharmaceutical research for lung, breast, and other solid tumor treatments. Also utilized in structure-activity relationship (SAR) studies to optimize inhibitor potency and selectivity.

Used as an intermediate in the synthesis of tyrosine kinase inhibitors, particularly in the development of anticancer agents. It plays a key role in targeting epidermal growth factor receptor (EGFR) pathways, which are involved in tumor cell proliferation and survival. Commonly applied in pharmaceutical research for lung, breast, and other solid tumor treatments. Also utilized in structure-activity relationship (SAR) studies to optimize inhibitor potency and selectivity.

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