4-Methyl-2-(trifluoromethyl)pyrimidine

98%

Reagent Code: #206339
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CAS Number 1017464-05-9

science Other reagents with same CAS 1017464-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.11 g/mol
Formula C₆H₅F₃N₂
badge Registry Numbers
MDL Number MFCD09881360
thermostat Physical Properties
Boiling Point 102.1±40.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with enhanced metabolic stability and binding affinity. Commonly employed in the manufacture of fungicides and herbicides due to the electron-withdrawing properties of the trifluoromethyl group, which improves lipophilicity and environmental persistence. Also utilized in medicinal chemistry for constructing pyrimidine-based scaffolds in drug discovery programs targeting kinase inhibitors and central nervous system agents.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,030.00
inventory 100mg
10-20 days ฿1,688.50
inventory 1g
10-20 days ฿15,580.00

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4-Methyl-2-(trifluoromethyl)pyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with enhanced metabolic stability and binding affinity. Commonly employed in the manufacture of fungicides and herbicides due to the electron-withdrawing properties of the trifluoromethyl group, which improves lipophilicity and environmental persistence. Also utilized in medicinal chemistry for constructing pyrimidine-ba

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of compounds with enhanced metabolic stability and binding affinity. Commonly employed in the manufacture of fungicides and herbicides due to the electron-withdrawing properties of the trifluoromethyl group, which improves lipophilicity and environmental persistence. Also utilized in medicinal chemistry for constructing pyrimidine-based scaffolds in drug discovery programs targeting kinase inhibitors and central nervous system agents.

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