N-(3-(2-(tert-Butyl)-5-(2-chloropyrimidin-4-yl)thiazol-4-yl)-2-fluorophenyl)-2,6-difluorobenzenesulfonamide

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Reagent Code: #218201
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CAS Number 1195768-23-0

science Other reagents with same CAS 1195768-23-0

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Weight 538.99 g/mol
Formula C₂₃H₁₈ClF₃N₄O₂S₂
badge Registry Numbers
MDL Number MFCD18447700
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. It plays a role in targeting specific signaling pathways involved in tumor growth and proliferation. Its structure enables selective binding to certain protein kinases, making it valuable in pharmaceutical research for designing drugs with improved efficacy and reduced side effects. Commonly applied in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,450.00
inventory 250mg
10-20 days ฿14,940.00
inventory 1g
10-20 days ฿24,740.00

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N-(3-(2-(tert-Butyl)-5-(2-chloropyrimidin-4-yl)thiazol-4-yl)-2-fluorophenyl)-2,6-difluorobenzenesulfonamide
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Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. It plays a role in targeting specific signaling pathways involved in tumor growth and proliferation. Its structure enables selective binding to certain protein kinases, making it valuable in pharmaceutical research for designing drugs with improved efficacy and reduced side effects. Commonly applied in medicinal chemistry for structure-activity relationship (SAR) studies to optimize dru

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in the development of anticancer agents. It plays a role in targeting specific signaling pathways involved in tumor growth and proliferation. Its structure enables selective binding to certain protein kinases, making it valuable in pharmaceutical research for designing drugs with improved efficacy and reduced side effects. Commonly applied in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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