3-Trifluoromethylpyridine

98%

Reagent Code: #240362
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CAS Number 3796-23-4

science Other reagents with same CAS 3796-23-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.10 g/mol
Formula C₆H₄F₃N
badge Registry Numbers
MDL Number MFCD00100032
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used in the synthesis of pharmaceuticals, particularly as a building block in the development of active pharmaceutical ingredients (APIs) due to the electron-withdrawing nature of the trifluoromethyl group, which can enhance metabolic stability and bioavailability. Commonly employed in agrochemicals for the production of herbicides and insecticides, where the pyridine ring combined with fluorine substituents improves lipophilicity and target specificity. Also utilized in materials science for designing organic semiconductors and liquid crystals, benefiting from its polarity and thermal stability. Frequently serves as an intermediate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, in both research and industrial settings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00
inventory 5g
10-20 days ฿860.00
inventory 25g
10-20 days ฿2,110.00
inventory 100g
10-20 days ฿5,950.00

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3-Trifluoromethylpyridine
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Used in the synthesis of pharmaceuticals, particularly as a building block in the development of active pharmaceutical ingredients (APIs) due to the electron-withdrawing nature of the trifluoromethyl group, which can enhance metabolic stability and bioavailability. Commonly employed in agrochemicals for the production of herbicides and insecticides, where the pyridine ring combined with fluorine substituents improves lipophilicity and target specificity. Also utilized in materials science for designing o

Used in the synthesis of pharmaceuticals, particularly as a building block in the development of active pharmaceutical ingredients (APIs) due to the electron-withdrawing nature of the trifluoromethyl group, which can enhance metabolic stability and bioavailability. Commonly employed in agrochemicals for the production of herbicides and insecticides, where the pyridine ring combined with fluorine substituents improves lipophilicity and target specificity. Also utilized in materials science for designing organic semiconductors and liquid crystals, benefiting from its polarity and thermal stability. Frequently serves as an intermediate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, in both research and industrial settings.

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