Ethyl 4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)benzoate

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Reagent Code: #183490
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CAS Number 641569-97-3

science Other reagents with same CAS 641569-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.37 g/mol
Formula C₁₉H₁₈N₄O₂
badge Registry Numbers
MDL Number MFCD11100712
thermostat Physical Properties
Boiling Point 546.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

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 proliferation. Shows potential in the development of anti-tumor agents due to its ability to modulate signaling pathways in malignant cells. Also employed in structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and selectivity. Its ester functionality allows for easy modification, making it valuable in medicinal chemistry for prodrug design and bioavailability enhancement.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,340.00
inventory 1g
10-20 days ฿780.00
inventory 10g
10-20 days ฿2,290.00

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Ethyl 4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)benzoate
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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 proliferation. Shows potential in the development of anti-tumor agents due to its ability to modulate signaling pathways in malignant cells. Also employed in structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and selectivity. Its ester functionality allows for easy modification, making it valuable in me

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell proliferation. Shows potential in the development of anti-tumor agents due to its ability to modulate signaling pathways in malignant cells. Also employed in structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and selectivity. Its ester functionality allows for easy modification, making it valuable in medicinal chemistry for prodrug design and bioavailability enhancement.

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