Isopropyl 2-((5-acrylamido-4-((2-(dimethylamino)ethyl)(methyl)amino)-2-methoxyphenyl)amino)-4-(1-methyl-1H-indol-3-yl)pyrimidine-5-carboxylate

98%

Reagent Code: #200661
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Alias TAK-788
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CAS Number 1847461-43-1

science Other reagents with same CAS 1847461-43-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 585.7 g/mol
Formula C₃₂H₃₉N₇O₄
inventory_2 Storage & Handling
Storage 2-8°C, inert gas, light-proof

description Product Description

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in targeted cancer therapies. Its structure enables selective binding to specific enzyme sites, making it valuable in drug development for oncology. Commonly employed in research settings to design compounds that modulate cell signaling pathways involved in tumor growth and proliferation. Also utilized in the formulation of photolabile protecting groups due to its responsive aromatic system, supporting controlled release mechanisms in biochemical applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,210.00
inventory 250mg
10-20 days ฿5,316.00
inventory 1g
10-20 days ฿23,930.00

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Isopropyl 2-((5-acrylamido-4-((2-(dimethylamino)ethyl)(methyl)amino)-2-methoxyphenyl)amino)-4-(1-methyl-1H-indol-3-yl)pyrimidine-5-carboxylate
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Used as a key intermediate in the synthesis of kinase inhibitors, particularly in targeted cancer therapies. Its structure enables selective binding to specific enzyme sites, making it valuable in drug development for oncology. Commonly employed in research settings to design compounds that modulate cell signaling pathways involved in tumor growth and proliferation. Also utilized in the formulation of photolabile protecting groups due to its responsive aromatic system, supporting controlled release mecha

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in targeted cancer therapies. Its structure enables selective binding to specific enzyme sites, making it valuable in drug development for oncology. Commonly employed in research settings to design compounds that modulate cell signaling pathways involved in tumor growth and proliferation. Also utilized in the formulation of photolabile protecting groups due to its responsive aromatic system, supporting controlled release mechanisms in biochemical applications.

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