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Merck
CN

V800294

高氯酸 溶液

0.1 N in acetic acid

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关于此项目

线性分子式:
HClO4
化学文摘社编号:
分子量:
100.46
UNSPSC Code:
12352300
PubChem Substance ID:
MDL number:
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产品名称

高氯酸 溶液, 0.1 N in acetic acid

InChI

1S/ClHO4/c2-1(3,4)5/h(H,2,3,4,5)

SMILES string

OCl(=O)(=O)=O

InChI key

VLTRZXGMWDSKGL-UHFFFAOYSA-N

product line

Vetec

form

liquid

concentration

0.1 N in acetic acid

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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

pictograms

Flame over circle

signalword

Danger

hcodes

pcodes

Hazard Classifications

Ox. Liq. 2

存储类别

5.1B - Oxidizing hazardous materials

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

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Perchloric Acid catalyzed aromatic mercuration in acetic acid solution. II. The Substitution Process
Kresge, A and Brennan, J
The Journal of Organic Chemistry, 32(3), 752-755 (1967)
Perchloric Acid-Acetic Acid: A Reagent System for Detosylation
Kudav, DP, et al.
Synthetic Communications, 17(10), 1185-1187 (1987)
John Greenwood et al.
ACS nano, 9(5), 5520-5535 (2015-04-22)
We shine light on the covalent modification of graphite and graphene substrates using diazonium chemistry under ambient conditions. We report on the nature of the chemical modification of these graphitic substrates, the relation between molecular structure and film morphology, and
Martin G Liebensteiner et al.
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
Dipanwita Das et al.
Journal of the American Chemical Society, 135(10), 4018-4026 (2013-02-28)
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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