CAS 887144-94-7
:1-(Trifluoromethyl)-1,2-benziodoxol-3(1H)-one
Description:
1-(Trifluoromethyl)-1,2-benziodoxol-3(1H)-one, with the CAS number 887144-94-7, is a chemical compound characterized by its unique structure that includes a benziodoxole moiety and a trifluoromethyl group. This compound is typically recognized for its role as a reagent in organic synthesis, particularly in the field of fluorination and oxidation reactions. The presence of the trifluoromethyl group enhances its reactivity and stability, making it a valuable intermediate in the synthesis of various fluorinated organic compounds. Additionally, the benziodoxole framework contributes to its electrophilic properties, allowing it to participate in diverse chemical transformations. The compound is generally handled with care due to its potential reactivity and the presence of fluorine, which can pose environmental and health risks. Overall, 1-(Trifluoromethyl)-1,2-benziodoxol-3(1H)-one is an important tool in synthetic chemistry, particularly for researchers focused on developing new fluorinated materials and pharmaceuticals.
Formula:C8H4F3IO2
InChI:InChI=1S/C8H4F3IO2/c9-8(10,11)12-6-4-2-1-3-5(6)7(13)14-12/h1-4H
SMILES:c1ccc2c(c1)C(=O)OI2C(F)(F)F
Synonyms:- 1-(Trifluoromethyl)-1,2-benziodoxol-3-(1H)-one(Togni's Reagent II)
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Found 5 products.
1-Trifluoromethyl-1,2-benziodoxol-3(1H)-one (contains 60% Diatomaceous earth)
CAS:Formula:C8H4F3IO2Color and Shape:White to Almost white powder to crystalMolecular weight:316.021-(Trifluoromethyl)-1,2-benziodoxol-3(1H)-one
CAS:Formula:C8H4F3IO2Purity:97%Color and Shape:SolidMolecular weight:316.0158Togni Reagent II
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications Used primarily as a reagent in trifluoromethylation reactions.<br>References Fantasia, S. et al.: J. Org. Chem., 75, 1779 (2010);<br></p>Formula:C8H4F3IO2Color and Shape:NeatMolecular weight:316.021-(Trifluoromethyl)-1,2-benziodoxol-3(1h)-one
CAS:<p>1-(Trifluoromethyl)-1,2-benziodoxol-3(1H)-one is a deuterated analog of the phenoxy radical. It has been shown to be a potent inhibitor of the apical radiation-induced chain reactions in mitochondria and chloroplasts. The deuterium isotope effect makes 1-(Trifluoromethyl)-1,2-benziodoxol-3(1H)-one more reactive than its non-deuterated counterpart. This increased reactivity leads to an increase in biological properties, such as toxicity studies and reaction mechanism. This drug also has modulating effects on sulfonic acids, which are important for many biological reactions.</p>Formula:C8H4F3IO2Purity:Min. 95 Area-%Color and Shape:White PowderMolecular weight:316.02 g/mol




