N-Methyl-1-(6-(trifluoromethyl)pyridin-3-yl)methanamine

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Reagent Code: #219932
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CAS Number 886364-80-3

science Other reagents with same CAS 886364-80-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.17 g/mol
Formula C₈H₉F₃N₂
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MDL Number MFCD07375086
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in agrochemicals for designing novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl group. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving nitrogen-containing heterocycles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,140.00
inventory 250mg
10-20 days ฿8,220.00

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N-Methyl-1-(6-(trifluoromethyl)pyridin-3-yl)methanamine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in agrochemicals for designing novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl group. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving nitrogen-containin

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in agrochemicals for designing novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl group. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving nitrogen-containing heterocycles.

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