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

Short Description:

Chemical Name: Methyl Trifluoromethanesulfonate

CAS: 333-27-7

Purity: >99.0% (GC)

Appearance: Colorless Transparent Liquid

High Quality, Commercial Production

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Description:

Shanghai 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

Chemical Properties:

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

Specifications:

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

Package & Storage:

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 moisture

Advantages:

FAQ:

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.