CAS 333-27-7
:Methanesulfonic acid, trifluoro-, methyl ester
Description:
Methanesulfonic acid, trifluoro-, methyl ester, commonly referred to as methyl trifluoromethanesulfonate, is an organofluorine compound characterized by its trifluoromethyl and methanesulfonate functional groups. It is a colorless to pale yellow liquid with a pungent odor. This compound is known for its high reactivity, particularly as an electrophile in organic synthesis, making it useful in various chemical reactions, including alkylation and acylation processes. Its trifluoromethyl group enhances its stability and lipophilicity, while the methanesulfonate moiety contributes to its ability to act as a leaving group in nucleophilic substitution reactions. Methanesulfonic acid, trifluoro-, methyl ester is soluble in polar organic solvents and is generally handled with care due to its corrosive nature and potential health hazards upon exposure. It is important to follow appropriate safety protocols when working with this compound, including the use of personal protective equipment and proper ventilation.
Formula:C2H3F3O3S
InChI:InChI=1/C2H3F3O3S/c1-8-9(6,7)2(3,4)5/h1H3
InChI key:InChIKey=OIRDBPQYVWXNSJ-UHFFFAOYSA-N
SMILES:S(C(F)(F)F)(OC)(=O)=O
Synonyms:- Methanesulfonic acid, 1,1,1-trifluoro-, methyl ester
- Methyl Trifluoromethanesulphonate
- Methyl triflate
- Methyl trifluoromethanesulfonate
- Methyltrifluormethansulfonat
- Nsc 270679
- Trifluorometanosulfonato De Metilo
- Trifluoromethanesulfonate de methyle
- Trifluoromethanesulfonate, Methyl
- Trifluoromethanesulfonic acid methyl ester
- Methanesulfonic acid, trifluoro-, methyl ester
- Methanesulfonicacid,trifluoro-,methylester
- 2-Chloro-4,5-Difluoro-Benzothiazole
- trifluoromethane-sulfinicacid,methylester
- trifluoro-methanesulfonicacimethylester
- methyltrifluoromethanesulfinate
- Methyl trifluoromethanesulphonate 98%
- Methyltrifluoromethanesulphonate98%
- Methyl trifluoromethanesulfonate ,96%
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Found 9 products.
Methyl Trifluoromethanesulfonate
CAS:Formula:C2H3F3O3SPurity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:164.10Methyl trifluoromethanesulfonate, 97%
CAS:<p>Methyl trifluoromethanesulfonate is used as a powerful methylating reagent in chemistry. Further, it is used in the conversion of amines to methyl ammonium triflates. In addition, it is also used in Suzuki reaction. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesa</p>Formula:C2H3F3O3SPurity:97%Molecular weight:164.1Methyl trifluoromethanesulfonate
CAS:Formula:C2H3F3O3SPurity:98%Color and Shape:LiquidMolecular weight:164.1036Ref: IN-DA003599
1g24.00€5g28.00€10g31.00€1kg504.00€25g56.00€50g67.00€100g115.00€250g211.00€500g271.00€Methyl trifluoromethanesulphonate
CAS:Methyl trifluoromethanesulphonateFormula:C2H3F3O3SPurity:98%Color and Shape: clear. colourless liquidMolecular weight:164.10362g/molMethyl trifluoromethanesulfonate
CAS:Formula:C2H3F3O3SPurity:99.0%Color and Shape:LiquidMolecular weight:164.1Trifluoromethanesulfonic Acid Methyl Ester
CAS:Controlled ProductFormula:C2H3F3O3SColor and Shape:NeatMolecular weight:164.10Methyl trifluoromethanesulfonate
CAS:<p>Methyl trifluoromethanesulfonate is a chemical compound that has been used in the synthesis of fluorescence probes and pharmaceuticals. It has an electron-withdrawing effect on the nitrogen atom, which enables it to react with amines. Methyl trifluoromethanesulfonate is a potent inhibitor of esterases, which are enzymes that hydrolyze esters. Methyl trifluoromethanesulfonate inhibits HIV infection by binding to gp120 and preventing receptor binding. This reaction also leads to conformational changes in gp120 and causes gp41 to insert into the membrane, disrupting fusion of viral and cellular membranes and inhibiting viral replication.</p>Formula:C2H3F3O3SPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:164.1 g/mol








