5-(Benzyloxy)pyrimidine-2-carbonitrile

95%

Reagent Code: #145686
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CAS Number 166672-22-6

science Other reagents with same CAS 166672-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.22 g/mol
Formula C₁₂H₉N₃O
thermostat Physical Properties
Boiling Point 406.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for constructing pyrimidine-based drug candidates with antiviral and anticancer properties. Also utilized in agrochemical research for designing novel pesticides due to its electron-deficient aromatic system that enhances binding to target enzymes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿640.00
inventory 100mg
10-20 days ฿1,550.00

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5-(Benzyloxy)pyrimidine-2-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for constructing pyrimidine-based drug candidates with antiviral and anticancer properties. Also utilized in agrochemical research for designing novel pesticides due to its electron-deficient aromatic system t

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for constructing pyrimidine-based drug candidates with antiviral and anticancer properties. Also utilized in agrochemical research for designing novel pesticides due to its electron-deficient aromatic system that enhances binding to target enzymes.

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