Home Sulfos 1-Butyl-3-methylimidazolium trifluoromethanesulfonate

1-Butyl-3-methylimidazolium trifluoromethanesulfonate

CAS No.:
174899-66-2
Catalog Number:
AG003E6H
Molecular Formula:
C9H15F3N2O3S
Molecular Weight:
288.2872
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25g
>98.0%(N)
1 week
United States
$589
- +
Product Description
Catalog Number:
AG003E6H
Chemical Name:
1-Butyl-3-methylimidazolium trifluoromethanesulfonate
CAS Number:
174899-66-2
Molecular Formula:
C9H15F3N2O3S
Molecular Weight:
288.2872
MDL Number:
MFCD03427620
IUPAC Name:
1-butyl-3-methylimidazol-3-ium;trifluoromethanesulfonate
InChI:
InChI=1S/C8H15N2.CHF3O3S/c1-3-4-5-10-7-6-9(2)8-10;2-1(3,4)8(5,6)7/h6-8H,3-5H2,1-2H3;(H,5,6,7)/q+1;/p-1
InChI Key:
FRZPYEHDSAQGAS-UHFFFAOYSA-M
SMILES:
[O-]S(=O)(=O)C(F)(F)F.CCCCn1cc[n+](c1)C
NSC Number:
746783
Properties
Complexity:
238  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
288.076g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
288.285g/mol
Monoisotopic Mass:
288.076g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
74.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
Role of the Hofmeister series in the formation of ionic-liquid-based aqueous biphasic systems. The journal of physical chemistry. B 20120621
Microwave-assisted separation of ionic liquids from aqueous solution of ionic liquids. Journal of chromatography. A 20101203
Optimization of lipase-catalyzed glucose ester synthesis in ionic liquids. Bioprocess and biosystems engineering 20100101
Anion configuration at the air/liquid interface of ionic liquid [bmim]OTf studied by sum-frequency generation spectroscopy. The journal of physical chemistry. B 20080925
Temperature-programed time-of-flight secondary ion mass spectrometry study of 1-butyl-3-methylimidazolium trifluoromethanesulfonate during glass-liquid transition, crystallization, melting, and solvation. The Journal of chemical physics 20080907
Properties