1,1,1-Trifluoro-n,n-dimethylmethanesulfonamide

98%

Reagent Code: #242979
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CAS Number 28048-17-1

science Other reagents with same CAS 28048-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.15 g/mol
Formula C₃H₆F₃NO₂S
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of trifluoromethyl-containing pharmaceuticals and agrochemicals due to its ability to introduce the trifluoromethyl group into organic molecules. It is also employed in the preparation of fluorinated surfactants and polymers, where the trifluoromethyl moiety enhances thermal stability, chemical resistance, and lipophobicity. Its reactivity makes it valuable in forming sulfonamide derivatives used in medicinal chemistry, particularly in the development of bioactive compounds with improved metabolic stability and membrane permeability. Additionally, it finds use in specialty solvents and as a reagent in organic transformations involving electrophilic trifluoromethylation.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,130.00
5g
10-20 days ฿3,680.00
10g
10-20 days ฿7,100.00
50g
10-20 days ฿29,800.00

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1,1,1-Trifluoro-n,n-dimethylmethanesulfonamide
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Used as a key intermediate in the synthesis of trifluoromethyl-containing pharmaceuticals and agrochemicals due to its ability to introduce the trifluoromethyl group into organic molecules. It is also employed in the preparation of fluorinated surfactants and polymers, where the trifluoromethyl moiety enhances thermal stability, chemical resistance, and lipophobicity. Its reactivity makes it valuable in forming sulfonamide derivatives used in medicinal chemistry, particularly in the development of bioact

Used as a key intermediate in the synthesis of trifluoromethyl-containing pharmaceuticals and agrochemicals due to its ability to introduce the trifluoromethyl group into organic molecules. It is also employed in the preparation of fluorinated surfactants and polymers, where the trifluoromethyl moiety enhances thermal stability, chemical resistance, and lipophobicity. Its reactivity makes it valuable in forming sulfonamide derivatives used in medicinal chemistry, particularly in the development of bioactive compounds with improved metabolic stability and membrane permeability. Additionally, it finds use in specialty solvents and as a reagent in organic transformations involving electrophilic trifluoromethylation.

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