Methyl Trifluoromethanesulfonate CAS 333-27-7 Purity >99.0% (GC) Factory

Chemical Name: Methyl Trifluoromethanesulfonate CAS: 333-27-7 Purity: >99.0% (GC)  Appearance: Colorless Transparent Liquid High Quality, Commercial Production E-Mail: alvin@ruifuchem.com

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Package: Bottle, 25kg/Barrel, or according to customer's requirement Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moistureShanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Methyl Trifluoromethanesulfonate (CAS: 333-27-7) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com
Item Specifications
Appearance Colorless Transparent Liquid
Purity / Analysis Method >99.0% (GC)   
Refractive Index n20/D 1.324~1.328
Infrared Spectrum Conforms to Structure
Test Standard Enterprise Standard

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Chemical Name Methyl Trifluoromethanesulfonate 
Synonyms Methyl Triflate; Trifluoromethanesulfonic Acid Methyl Ester
CAS Number 333-27-7
CAT Number RF-PI2095
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C2H3F3O3S
Molecular Weight 164.10  
Boiling Point 94.0~99.0℃(lit.)
Density 1.45 g/mL at 25℃(lit.) 
Sensitivity Moisture Sensitive
Brand Ruifu Chemical

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Application:

Methyl Trifluoromethanesulfonate (CAS: 333-27-7) 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. Methyl trifluoromethanesulfonic acid is a very useful trifluoromethanesulfonic acid ester reagent in organic synthesis, often used as alkylation reagent. Trifluoromethanesulfonic ester compounds of trifluoromethanesulfonic ester have strong electron absorption ability, reactivity than conventional alkylation reagents such as than chlorine or alkyl sulfonate much higher. Due to their high activity, only methyl trifluoromethanesulfonic acid is relatively stable. The other trifluoromethanesulfonic acid esters are prone to elimination, rearrangement and other side reactions, requiring synthesis and post-treatment under mild conditions. Organic synthesis, pharmaceutical synthesis intermediates.

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