N-isopropyl-4-(trifluoromethyl)pyrimidin-2-amine

97%

Reagent Code: #214718
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CAS Number 651292-53-4

science Other reagents with same CAS 651292-53-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.1799 g/mol
Formula C₈H₁₀N₃F₃
thermostat Physical Properties
Boiling Point 242.9±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.264±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of small molecule therapeutics targeting inflammatory diseases and certain viral infections. Its trifluoromethyl group contributes to improved lipophilicity and bioavailability in final active ingredients.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿23,100.00
N-isopropyl-4-(trifluoromethyl)pyrimidin-2-amine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of small molecule therapeutics targeting inflammatory diseases and certain viral infections. Its trifluoromethyl group contributes to improved lipophilicity and bioavailability in fin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of small molecule therapeutics targeting inflammatory diseases and certain viral infections. Its trifluoromethyl group contributes to improved lipophilicity and bioavailability in final active ingredients.

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