Methyl 3,3,3-trifluoro-2,2-dimethylpropanoate

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Reagent Code: #207860
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CAS Number 1188911-72-9

science Other reagents with same CAS 1188911-72-9

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Weight 170.13 g/mol
Formula C₆H₉F₃O₂
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MDL Number MFCD18253569
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its trifluoromethyl group contributes to increased lipophilicity and electron-withdrawing effects, making it valuable in modifying drug candidates for improved pharmacokinetic properties. Also employed in the preparation of specialty monomers for fluoropolymers, where it imparts thermal and chemical resistance to the resulting materials. Additionally, it serves in organic synthesis as a building block for introducing the gem-dimethyl-trifluoropropionate moiety in active ingredients of crop protection agents.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿5,040.00
inventory 10g
10-20 days ฿10,560.00
inventory 25g
10-20 days ฿25,120.00

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Methyl 3,3,3-trifluoro-2,2-dimethylpropanoate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its trifluoromethyl group contributes to increased lipophilicity and electron-withdrawing effects, making it valuable in modifying drug candidates for improved pharmacokinetic properties. Also employed in the preparation of specialty monomers for fluoropolymers, where it imparts thermal and chemical resistance to

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its trifluoromethyl group contributes to increased lipophilicity and electron-withdrawing effects, making it valuable in modifying drug candidates for improved pharmacokinetic properties. Also employed in the preparation of specialty monomers for fluoropolymers, where it imparts thermal and chemical resistance to the resulting materials. Additionally, it serves in organic synthesis as a building block for introducing the gem-dimethyl-trifluoropropionate moiety in active ingredients of crop protection agents.

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