trifluoromethanesulfonic acid-1H-imidazole (1:1)

Names

[ 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

Imidazole
Methyl trifluoromethanesulfonate
triflic anhydride
Trifluoromethanesulfonic acid
tert-butylphenylphosphinic imidazolidide

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

Benzimidazolium triflate-activated synthesis of (6-4) photoproduct-containing oligonucleotides and its application.

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...

n-(2-Bromo-4-fluorobenzyl)-1-(4-methylmorpholin-2-yl)methanamine
8-(4-methoxyphenyl)-1,3-dimethyl-5-(3-methylbutyl)-4aH-purino[8,9-c][1,2,4]triazol-1-ium-2,4-dione
1,3-Dimethyl-8-(4-methylphenyl)-5-[(2-methylphenyl)methyl]-4a,9a-dihydropurino[8,9-c][1,2,4]triazole-2,4-dione
1-(2,5-dimethoxyphenyl)-2-(6-propan-2-yl-1,3-benzothiazol-2-yl)-4a,5,6,7,8,8a-hexahydro-1H-chromeno[2,3-c]pyrrole-3,9-dione
2-(6-ethoxy-1,3-benzothiazol-2-yl)-1-(4-fluorophenyl)-7-methyl-4a,5,6,7,8,8a-hexahydro-1H-chromeno[2,3-c]pyrrole-3,9-dione
2-(6-chloro-1,3-benzothiazol-2-yl)-1-(5-methylfuran-2-yl)-4a,5,6,7,8,8a-hexahydro-1H-chromeno[2,3-c]pyrrole-3,9-dione
1-(4-tert-butylphenyl)-7-ethyl-2-(5-methyl-1,2-oxazol-3-yl)-4a,5,6,7,8,8a-hexahydro-1H-chromeno[2,3-c]pyrrole-3,9-dione
7-ethyl-2-(5-methyl-1,2-oxazol-3-yl)-1-(3,4,5-trimethoxyphenyl)-4a,5,6,7,8,8a-hexahydro-1H-chromeno[2,3-c]pyrrole-3,9-dione
1-[3-[(4-chlorophenyl)methoxy]phenyl]-7-fluoro-2-(5-methyl-1,2-oxazol-3-yl)-4a,5,6,7,8,8a-hexahydro-1H-chromeno[2,3-c]pyrrole-3,9-dione
2-(6-ethoxy-1,3-benzothiazol-2-yl)-1-(2-fluorophenyl)-7-methyl-4a,5,6,7,8,8a-hexahydro-1H-chromeno[2,3-c]pyrrole-3,9-dione

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