515876
Imidazole trifluoromethanesulfonate salt
97%
Synonym(s):
Imidazolium triflate
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About This Item
Empirical Formula (Hill Notation):
C3H4N2 · CHF3O3S
CAS Number:
Molecular Weight:
218.15
UNSPSC Code:
12352005
eCl@ss:
39161001
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Assay:
97%
SMILES string
c1c[nH]cn1.OS(=O)(=O)C(F)(F)F
InChI
1S/C3H4N2.CHF3O3S/c1-2-5-3-4-1;2-1(3,4)8(5,6)7/h1-3H,(H,4,5);(H,5,6,7)
InChI key
JNJFONBBNLVENC-UHFFFAOYSA-N
assay
97%
mp
189-193 °C (lit.)
functional group
fluoro, triflate
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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S Iwai et al.
Nucleic acids research, 27(11), 2299-2303 (1999-05-15)
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 length increased. The by-products were the major product when a 49mer was synthesized on a 40
Stéphane Bernier et al.
Bioorganic & medicinal chemistry, 13(1), 69-75 (2004-12-08)
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 inhibitor (K(i) = 15 nM) whereas L-aspartol adenylate is a weaker inhibitor (K(i) = 45 microM) with respect
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