trifluoromethanesulfonic acid-1H-imidazole (1:1)
Names
[ CAS No. ]:
29727-06-8
[ Name ]:
trifluoromethanesulfonic acid-1H-imidazole (1:1)
[Synonym ]:
Imidazole trifluoromethanesulfonate salt
imidazole triflate
imidazolium trifluoromethanesulfonate
MFCD00035430
Imidazole trifluoromethanesulfonate
Imidazolium triflate
Chemical & Physical Properties
[ Boiling Point ]:
162ºC at 760 mmHg
[ Melting Point ]:
189-193ºC(lit.)
[ Molecular Formula ]:
C4H5F3N2O3S
[ Molecular Weight ]:
218.15400
[ Flash Point ]:
185.8ºC
[ Exact Mass ]:
217.99700
[ PSA ]:
91.43000
[ LogP ]:
1.88450
[ Vapour Pressure ]:
1.14mmHg at 25°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ HS Code ]:
2933290090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933290090
[ Summary ]:
2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Nucleic Acids Res. 27(11) , 2299-303, (1999)
In the solid-phase synthesis of oligonucleotides containing the pyrimidine(6-4)pyrimidone photoproduct using a dinucleotide building block, considerable amounts of by-products were found as the chain ...
Synthesis and aminoacyl-tRNA synthetase inhibitory activity of aspartyl adenylate analogs.Bioorg. Med. Chem. 13(1) , 69-75, (2005)
Three nonhydrolyzable aspartyl adenylate analogs have been prepared and tested as inhibitors of E. coli aspartyl-tRNA synthetase. 5'-O-[N-(L-Aspartyl)sulfamoyl]adenosine is a potent competitive inhibi...