158534
Trifluoromethanesulfonic acid
reagent grade, 98%
Synonym(s):
TFMSA, Triflic acid
About This Item
Recommended Products
grade
reagent grade
Quality Level
vapor density
5.2 (vs air)
vapor pressure
8 mmHg ( 25 °C)
Assay
98%
form
liquid
refractive index
n20/D 1.327 (lit.)
bp
162 °C (lit.)
density
1.696 g/mL at 25 °C (lit.)
functional group
fluoro
triflate
SMILES string
OS(=O)(=O)C(F)(F)F
InChI
1S/CHF3O3S/c2-1(3,4)8(5,6)7/h(H,5,6,7)
InChI key
ITMCEJHCFYSIIV-UHFFFAOYSA-N
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General description
Application
- Friedel-Crafts acylation of aromatic compounds with methyl benzoate.
- Addition reaction of dialkyl disulfides to terminal alkynes.
- Synthesis of a single cyclic tetrasiloxane containing propylammonium trifluoromethanesulfonate and methyl side-chain groups (Am-CyTS).
- Preparation of starting reagents for the synthesis of fluorinated 2,5-substituted 1-ethyl-1H-benzimidazole derivatives.
- Synthesis of aryl triflates, the lactonization of alkenoic acids, and the formation of E-alkenes.
accessory
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
>332.1 °F - Pensky-Martens closed cup
Flash Point(C)
> 166.7 °C - Pensky-Martens closed cup
Personal Protective Equipment
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Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
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Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
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