2,4-Dichloroquinazoline-8-carbonitrile

95%

Reagent Code: #180070
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CAS Number 1150617-71-2

science Other reagents with same CAS 1150617-71-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.05 g/mol
Formula C₉H₃Cl₂N₃
badge Registry Numbers
MDL Number MFCD12024546
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating compounds with high biological activity. Commonly employed in research settings to design drugs targeting tyrosine kinases involved in tumor growth and inflammation. Also utilized in agrochemical research for developing novel pesticides due to its electron-deficient aromatic system that enhances binding to biological targets.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿31,080.00
inventory 250mg
10-20 days ฿51,580.00

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2,4-Dichloroquinazoline-8-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating compounds with high biological activity. Commonly employed in research settings to design drugs targeting tyrosine kinases involved in tumor growth and inflammation. Also utilized in agrochemical research for developing novel pesticides due to its electron-deficient aromatic system that enhan
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating compounds with high biological activity. Commonly employed in research settings to design drugs targeting tyrosine kinases involved in tumor growth and inflammation. Also utilized in agrochemical research for developing novel pesticides due to its electron-deficient aromatic system that enhances binding to biological targets.
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