CAS 6226-25-1

2,2,2-Trifluoroethyl trifluoromethanesulfonate

Description:

2,2,2-Trifluoroethyl trifluoromethanesulfonate, with the CAS number 6226-25-1, is a chemical compound characterized by its trifluoromethyl and sulfonate functional groups. This substance is typically a colorless liquid at room temperature and is known for its high volatility and low viscosity. It exhibits strong electrophilic properties due to the presence of the trifluoromethanesulfonate group, making it a useful reagent in organic synthesis, particularly in the formation of carbon-fluorine bonds. The trifluoroethyl group contributes to its stability and lipophilicity, enhancing its utility in various chemical reactions. Additionally, this compound is recognized for its potential applications in pharmaceuticals and agrochemicals, where it can serve as an intermediate in the synthesis of more complex molecules. However, it is important to handle this substance with care due to its potential toxicity and environmental impact, necessitating appropriate safety measures during use and disposal.

Formula: C₃H₂F₆O₃S

InChI: InChI=1S/C3H2F6O3S/c4-2(5,6)1-12-13(10,11)3(7,8)9/h1H2

InChI key: InChIKey=RTMMSCJWQYWMNK-UHFFFAOYSA-N

SMILES: S(C(F)(F)F)(OCC(F)(F)F)(=O)=O

Synonyms:

• 2,2,2-Trifluoroethyl triflate
• 2,2,2-Trifluoroethyl trifluoromethanesulphonate
• 2,2,2-Trifluoroethyl trifluoromethylsulfonate
• Ethanol, 2,2,2-trifluoro-, trifluoromethanesulfonate
• Methanesulfonic acid, 1,1,1-trifluoro-, 2,2,2-trifluoroethyl ester
• Methanesulfonic acid, trifluoro-, 2,2,2-trifluoroethyl ester
• Trifluoromethanesulfonic acid 2,2,2-trifluoroethyl ester
• 2,2,2-Trifluoroethyl trifluoromethanesulfonate

2,2,2-Trifluoroethyl Trifluoromethanesulfonate

CAS: 6226-25-1

Formula: C₃H₂F₆O₃S

Purity: >97.0%(GC)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 232.10

Ref: 3B-T1604

2,2,2-Trifluoroethyl trifluoromethanesulfonate, 95%

CAS: 6226-25-1

2,2,2-Trifluoroethyl trifluoromethanesulfonate is a powerful trifluoroethylating agent which is useful for synthesis of fluorinated amino acids. It is used as a reagent in thenantioselective preparation of cyclic N-aryl hydroxamic acids via phase-transfer catalyzed alkylation of nitrobenzyl bromides

Formula: C₃H₂F₆O₃S

Purity: 95%

Color and Shape: Clear colorless to yellow, Liquid

Molecular weight: 232.10

Ref: 02-H61603

2,2,2-Trifluoroethyltrifluoromethanesulfonate

CAS: 6226-25-1

Formula: C₃H₂F₆O₃S

Purity: 95%

Color and Shape: Liquid

Molecular weight: 232.1016

Ref: IN-DA0032W7

2,2,2-Trifluoroethyl trifluoromethanesulphonate

CAS: 6226-25-1

2,2,2-Trifluoroethyl trifluoromethanesulphonate

Formula: C₃H₂F₆O₃S

Purity: 97%

Color and Shape: clear. colourless liquid

Molecular weight: 232.10g/mol

Ref: 54-PC3903

2,2,2-Trifluoroethyl trifluoromethanesulfonate

CAS: 6226-25-1

Formula: C₃H₂F₆O₃S

Purity: 97%

Color and Shape: Liquid

Molecular weight: 232.1

Ref: 10-F008628

2,2,2-Trifluoroethyl Triflate

Controlled Product

CAS: 6226-25-1

Applications A fluorine-containing alkyl alkanesulfonate with cyctotoxity towards cultured leukemia L1210 cells.
References Ohta, Y. et al.: Chem. Pharmac. Bull., 36, 2410 (1988);

Formula: C₃H₂F₆O₃S

Color and Shape: Neat

Molecular weight: 232.1

Ref: TR-T790300

2,2,2-Trifluoroethyl triflate

CAS: 6226-25-1

2,2,2-Trifluoroethyl triflate (TFE) is a gaseous compound that is used as a reagent in organic synthesis. It reacts with nucleophiles to form fluorinated products. The reaction can be observed by spectroscopic analysis and is useful for the synthesis of fluorinated molecules. 2,2,2-Trifluoroethyl triflate has been shown to react with arginine methyl groups to form methylated arginine derivatives. This reaction is an example of a nucleophilic substitution reaction that occurs at an electrophilic carbon atom.

Formula: C₃H₂F₆O₃S

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 232.1 g/mol

Ref: 3D-FT28461