m-(2,2,2-trifluoroacetyl)phenylamino 2,2-dimethylpropionate

≥95%

Reagent Code: #204170
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CAS Number 1645279-91-9

science Other reagents with same CAS 1645279-91-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.25 g/mol
Formula C₁₃H₁₄F₃NO₃
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for selective transformations, making it valuable in constructing complex molecules. The trifluoroacetyl group enhances reactivity and can act as a directing group in metal-catalyzed reactions. It is also employed in the preparation of bioactive compounds where fluorine substitution improves metabolic stability and lipophilicity. Commonly utilized in research settings for designing new active ingredients in crop protection agents and medicinal candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,020.00
inventory 1g
10-20 days ฿5,760.00
inventory 5g
10-20 days ฿20,160.00

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m-(2,2,2-trifluoroacetyl)phenylamino 2,2-dimethylpropionate
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for selective transformations, making it valuable in constructing complex molecules. The trifluoroacetyl group enhances reactivity and can act as a directing group in metal-catalyzed reactions. It is also employed in the preparation of bioactive compounds where fluorine substitution improves metabolic stability and lipophilicity. Commonly utilized in research se

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for selective transformations, making it valuable in constructing complex molecules. The trifluoroacetyl group enhances reactivity and can act as a directing group in metal-catalyzed reactions. It is also employed in the preparation of bioactive compounds where fluorine substitution improves metabolic stability and lipophilicity. Commonly utilized in research settings for designing new active ingredients in crop protection agents and medicinal candidates.

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