Methyl Trifluoromethanesulfonate - CAS# 333-27-7
Synonym
Methyl Triflate
CAS #
333-27-7
Molecular Formula
C2H3F3O3S
Molecular Weight
164.1
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Know More About Methyl Trifluoromethanesulfonate
With the CAS number 333-27-7, methyl trifluoromethanesulfonate, often known as methyl triflate, is an exceptionally versatile chemical molecule. It is made from methyl fluorosulfonate (FSO2OCH3) and is a powerful methylating agent in a variety of chemical processes.
The ability of methyl trifluoromethanesulfonate to add a methyl group (-CH3) onto nucleophilic compounds makes it an indispensable reagent in chemical synthesis. The existence of the triflatefunctional group (-SO3CF3), which readily conducts nucleophilic substitution processes, accounts for its reactivity.
Methyl triflate, as a methylating agent, is especially beneficial in the alkylation of different nucleophiles such as amines, alcohols, and phenols. The methylation compounds that arise frequently have changed characteristics, increased bioactivity, or better stability, making them significant building blocks in the pharmaceutical and agrochemical industries.
Methyl trifluoromethanesulfonate dissolves readily in ordinary organic solvents, making it simple to include in reaction mixes. Due to its responsiveness and the ability to dissolve, it is a popular option in both solution-phase and solid-phase organic synthesis.
However, because of the possible risks, methyl trifluoromethanesulfonate should be handled with caution. It is a highly reactive and poisonous substance that must be handled with extreme caution. Wearing protective equipment, such as gloves and safety glasses, and performing operations in a well-ventilated space are recommended.
Finally, methyl trifluoromethanesulfonate (CAS number 333-27-7), often known as methyl triflate, is a strong methylating agent utilised in chemical synthesis. It is useful in the manufacturing of medicines and agrochemicals due to its capacity to insert a methyl group onto nucleophilic molecules. Methyl triflate is used in alkylation processes to change the characteristics of target compounds. When working with this reactive and dangerous substance, however, measures must be taken.