N-allyl-2,2,2-trifluoroacetamide

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Reagent Code: #216928
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CAS Number 383-65-3

science Other reagents with same CAS 383-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.104 g/mol
Formula C₅H₆F₃NO
badge Registry Numbers
MDL Number MFCD00780948
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of the trifluoromethyl group, which enhances metabolic stability and lipophilicity. The allyl group allows for further functionalization via cross-coupling or olefin transformation reactions. Commonly employed in the development of bioactive molecules where fluorine substitution improves potency or pharmacokinetic properties. Also utilized in research settings for building blocks in heterocyclic chemistry and in the preparation of specialty monomers for functional polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,430.00
inventory 250mg
10-20 days ฿2,180.00
inventory 1g
10-20 days ฿8,500.00
inventory 5g
10-20 days ฿29,880.00

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N-allyl-2,2,2-trifluoroacetamide
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Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of the trifluoromethyl group, which enhances metabolic stability and lipophilicity. The allyl group allows for further functionalization via cross-coupling or olefin transformation reactions. Commonly employed in the development of bioactive molecules where fluorine substitution improves potency or pharmacokinetic properties. Also utilized in research settings for building blocks in heterocyclic

Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of the trifluoromethyl group, which enhances metabolic stability and lipophilicity. The allyl group allows for further functionalization via cross-coupling or olefin transformation reactions. Commonly employed in the development of bioactive molecules where fluorine substitution improves potency or pharmacokinetic properties. Also utilized in research settings for building blocks in heterocyclic chemistry and in the preparation of specialty monomers for functional polymers.

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