2,2,2-Trifluoro-1-(5-methylpyridin-2-yl)ethanone

≥95%

Reagent Code: #241748
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CAS Number 1060801-56-0

science Other reagents with same CAS 1060801-56-0

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Weight 189.14 g/mol
Formula C₈H₆F₃NO
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MDL Number MFCD13188989
inventory_2 Storage & Handling
Storage Store in inert gas at room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its trifluoromethyl ketone group enables strong hydrogen bonding and dipole interactions, enhancing binding affinity to target enzymes. Commonly employed in medicinal chemistry for optimizing metabolic stability and improving pharmacokinetic properties of drug candidates. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,570.00
inventory 250mg
10-20 days ฿19,050.00

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2,2,2-Trifluoro-1-(5-methylpyridin-2-yl)ethanone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its trifluoromethyl ketone group enables strong hydrogen bonding and dipole interactions, enhancing binding affinity to target enzymes. Commonly employed in medicinal chemistry for optimizing metabolic stability and improving pharmacokinetic properties of drug candidates. Also utilized in agrochemical research for designing novel pesticides with imp

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its trifluoromethyl ketone group enables strong hydrogen bonding and dipole interactions, enhancing binding affinity to target enzymes. Commonly employed in medicinal chemistry for optimizing metabolic stability and improving pharmacokinetic properties of drug candidates. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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