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product line
Vetec™
form
liquid
concentration
0.1 N in acetic acid
SMILES string
OCl(=O)(=O)=O
InChI
1S/ClHO4/c2-1(3,4)5/h(H,2,3,4,5)
InChI key
VLTRZXGMWDSKGL-UHFFFAOYSA-N
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Application
Perchloric acid (in acetic acid) can be used as a detosylating agent for the deprotection of the tosyl functional groups in p-methyl benzene sulfonyl derivatives of primary, secondary aryl amines, and chiral aminoketones. It can also be used in the aromatic mercuration reaction.
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
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Perchloric Acid-Acetic Acid: A Reagent System for Detosylation
Synthetic Communications, 17(10), 1185-1187 (1987)
Perchloric Acid catalyzed aromatic mercuration in acetic acid solution. II. The Substitution Process
The Journal of Organic Chemistry, 32(3), 752-755 (1967)
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Science (New York, N.Y.), 340(6128), 85-87 (2013-04-06)
Perchlorate and chlorate anions [(per)chlorate] exist in the environment from natural and anthropogenic sources, where they can serve as electron acceptors for bacteria. We performed growth experiments combined with genomic and proteomic analyses of the hyperthermophile Archaeoglobus fulgidus that show
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Catalytic four-electron reduction of O2 by ferrocene (Fc) and 1,1'-dimethylferrocene (Me2Fc) occurs efficiently with a dinuclear copper(II) complex [Cu(II)2(XYLO)(OH)](2+) (1), where XYLO is a m-xylene-linked bis[(2-(2-pyridyl)ethyl)amine] dinucleating ligand with copper-bridging phenolate moiety], in the presence of perchloric acid (HClO4) in
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