(2-(Trifluoromethyl)pyridin-4-yl)methanamine

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Reagent Code: #238213
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CAS Number 916304-20-6

science Other reagents with same CAS 916304-20-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.1424 g/mol
Formula C₇H₇F₃N₂
badge Registry Numbers
MDL Number MFCD11100735
thermostat Physical Properties
Boiling Point 197.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.293±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, 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 enables strong binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemicals to improve metabolic stability and bioavailability of active ingredients. The trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing long-acting compounds.

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inventory 5g
10-20 days ฿335,590.00

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(2-(Trifluoromethyl)pyridin-4-yl)methanamine
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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 enables strong binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemicals to improve metabolic stability and bioavailability of active ingredients. The trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing long-acting compounds.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables strong binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemicals to improve metabolic stability and bioavailability of active ingredients. The trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing long-acting compounds.

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