145022-44-2 | 1-Ethyl-3-methylimidazolium trifluoromethanesulfonate

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$18.00	$12.00
10g	98%	in stock	$29.00	$21.00
25g	98%	in stock	$44.00	$31.00

Description

• Catalog Number: AB58309
• Chemical Name: 1-Ethyl-3-methylimidazolium trifluoromethanesulfonate
• CAS Number: 145022-44-2
• Molecular Formula: C7H11F3N2O3S
• Molecular Weight: 260.234
• MDL Number: MFCD00210008
• SMILES: FC(S(=O)(=O)[O-])(F)F.CCn1cc[n+](c1)C

Computed Properties

• Complexity: 218
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1

Upstream Synthesis Route

1-Ethyl-3-methyl-1H-imidazolium trifluoromethanesulfonate, commonly referred to as $name$, serves as a versatile ionic liquid in chemical synthesis. Due to its unique properties, this compound has found wide application as a reaction medium and catalyst in various organic reactions.In chemical synthesis, $name$ can act as a powerful solvent for the dissolution and reaction of both organic and inorganic compounds. Its high thermal stability and low volatility make it ideal for carrying out reactions at elevated temperatures. Additionally, its ability to dissolve a wide range of organic and inorganic compounds enhances its utility in various synthetic processes.Moreover, 1-Ethyl-3-methyl-1H-imidazolium trifluoromethanesulfonate has been recognized for its catalytic properties in promoting numerous chemical transformations. It can facilitate reactions such as esterifications, oxidations, and metal-catalyzed processes, thereby accelerating reaction rates and improving yields. Its effectiveness as a catalyst can be attributed to its unique structure and functional groups, which enable it to interact with reactants and stabilize intermediates.Overall, the application of $name$ in chemical synthesis offers researchers and chemists a valuable tool for conducting a wide range of reactions efficiently and selectively. By harnessing its solvent and catalytic capabilities, this compound contributes to the advancement of synthetic methodologies and the development of novel chemical compounds.

Literature

• Comparing reduced partial charge models with polarizable simulations of ionic liquids.

  Physical chemistry chemical physics : PCCP 20120307

• Ion-pair structure of vaporized ionic liquid studied by matrix-isolation FTIR spectroscopy with DFT calculations: a case of 1-ethyl-3-methylimidazolium trifluoromethanesulfonate.

  The journal of physical chemistry. A 20101209