4-Methoxy-2-(trifluoromethyl)pyridine

95%

Reagent Code: #119466
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CAS Number 1065103-97-0

science Other reagents with same CAS 1065103-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.12 g/mol
Formula C₇H₆F₃NO
badge Registry Numbers
MDL Number MFCD11054356
thermostat Physical Properties
Boiling Point 170.8±40.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active compounds. Its unique structure, featuring a methoxy group and a trifluoromethyl group on a pyridine ring, makes it valuable for developing molecules with enhanced biological activity and stability. In pharmaceuticals, it is often employed in the creation of drugs targeting specific diseases, including anti-inflammatory and anti-cancer agents. In agrochemicals, it serves as a building block for designing pesticides and herbicides, leveraging its ability to improve the efficacy and selectivity of these products. Additionally, its trifluoromethyl group contributes to increased lipophilicity, which can enhance the bioavailability of the final compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,514.00
inventory 250mg
10-20 days ฿6,489.00
inventory 100mg
10-20 days ฿3,825.00

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4-Methoxy-2-(trifluoromethyl)pyridine
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This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active compounds. Its unique structure, featuring a methoxy group and a trifluoromethyl group on a pyridine ring, makes it valuable for developing molecules with enhanced biological activity and stability. In pharmaceuticals, it is often employed in the creation of drugs targeting specific diseases, including anti-inflammatory and anti-cancer agents. In agrochemicals, it serves as a building block for designing pesticides and herbicides, leveraging its ability to improve the efficacy and selectivity of these products. Additionally, its trifluoromethyl group contributes to increased lipophilicity, which can enhance the bioavailability of the final compounds.
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