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

Suppliers

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

  • 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...


More Articles


Related Compounds

  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • Methyl 3-{[4-(benzyloxy)phenyl]sulfamoyl}-4-(4-methylphenyl)thiophene-2-carboxylate
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • 7-(2-Fluoro-4-iodo-phenylamino)-benzo[d]isothiazole-6-carboxylic acid
  • 2-(Difluoromethoxy)-4-(2-oxopropyl)benzaldehyde
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde