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2,6-Diphenylpyrylium perchlorate is a chemical compound with the molecular formula C20H15ClO4N. It is a derivative of pyrylium, a heterocyclic aromatic compound containing a pyrylium ring, which is a six-membered ring with one oxygen atom and five carbon atoms. The compound is characterized by the presence of two phenyl groups (C6H5) attached to the 2nd and 6th positions of the pyrylium ring. The perchlorate ion (ClO4-) is a counterion, which balances the positive charge of the pyrylium ring. 2,6-DiphenylpyryliuM perchlorate is often used in organic synthesis and as a reagent in various chemical reactions. It is important to note that perchlorate salts can be hazardous and should be handled with care due to their potential to form explosive compounds under certain conditions.

3558-68-7

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3558-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3558-68-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3558-68:
(6*3)+(5*5)+(4*5)+(3*8)+(2*6)+(1*8)=107
107 % 10 = 7
So 3558-68-7 is a valid CAS Registry Number.

3558-68-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diphenylpyrilium perchlorate

1.2 Other means of identification

Product number -
Other names 2,6-DiphenylpyryliuM perchlorate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3558-68-7 SDS

3558-68-7Relevant academic research and scientific papers

Method for manufacturing organic electronic devices

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Page/Page column 7, (2017/11/09)

The present invention relates to a method for manufacturing organic electronic devices including a dipyrannylidene film as an anodic interface layer, the method being carried out in a vacuum and without any exposure to air. The invention also relates to o

Selective and sensitive chromofluorogenic detection of the sulfite anion in water using hydrophobic hybrid organic-inorganic silica nanoparticles

Santos-Figueroa, Luis Enrique,Gimenez, Cristina,Agostini, Alessandro,Aznar, Elena,Marcos, Maria D.,Sancenon, Felix,Martinez-Manez, Ramon,Amoros, Pedro

supporting information, p. 13712 - 13716 (2014/01/06)

In water and wine: Chromofluorogenic detection of the sulfite anion in pure water was accomplished by using a new hybrid organic-inorganic material that contained a probe entrapped in hydrophobic biomimetic cavities. This material was used for the detecti

An instantaneous and highly selective chromofluorogenic chemodosimeter for fluoride anion detection in pure water

Elsayed, Sameh,Agostini, Alessandro,Santos-Figueroa, Luis E.,Martinez-Manez, Ramon,Sancenon, Felix

, p. 58 - 62 (2014/03/21)

The fast and the fluoride: A pyridine derivative functionalized with ferf-butyl-dimethylsilyl ether has been synthesized and used as a selective chromofluoro-genic fluoride sensor in water/cetyltri-methylammonium bromide solutions. The chromofluorogenic r

Hg2+ and Cu2+ selective detection using a dual channel receptor based on thiopyrylium scaffoldings

ábalos, Tatiana,Jiménez, Diego,Martínez-Má?ez, Ramón,Ros-Lis, Jose Vicente,Royo, Santiago,Sancenón, Félix,Soto, Juan,Costero, Ana M.,Gil, Salvador,Parra, Margarita

supporting information; experimental part, p. 3885 - 3888 (2009/09/30)

2,4,6-Triphenylthiopyrylium functionalized with an aza-oxa-thia macrocycle is able to selectively recognize Hg2+ cation by a color change and Cu2+ cation by a remarkable significant emission enhancement.

The use of N,N-dialkyltrimethylsilylamines in the synthesis of pentamethinium salts

Korinek, Marek,Rybackova, Marketa,Boehm, Stanislav

scheme or table, p. 1291 - 1296 (2009/12/07)

N,N-Dialkyltrimethylsilylamines were used for the synthesis of a series of pentamethinium salts starting from 2,6-disubstituted or 2,4,6-trisubstituted pyrylium salts, N-substituted 5-aminopenta-2,4-dienals or N-substituted 5-aminopenta-2,4-dien-1-ones. The reactions proceed smoothly under mild conditions, furnishing the desired products in good yields. Georg Thieme Verlag Stuttgart.

Reactions of 3-Thia(Selena)Pentane-1,5-Diones with Lewis Acids

Zhukov, Oleg I.,Drevko, Boris I.

, p. 663 - 666 (2007/10/03)

3-Thia(selena)pentane-1,5-diones react with Lewis acids by hetero-atom. In these reactions soft Lewis acids such as tin tetrachloride and antimony pentachloride form adducts but hard Lewis acid such as phosphorus pentachloride oxidizes chalcogen atom of 3

Electrophilic Reactions of Carbonyl Compounds and their Derivatives. VI. Vinyl Ethers and Chlorinated Hydrocarbons in the Synthesis of Pyrylium Salts

Luk'yanov, S. M.

, p. 794 - 800 (2007/10/03)

Two- and three-component condensations of α-ethoxystyrene with carbonyl compounds and their derivatives serving as a source of heterocarbenium and hydroxyallyl cations are studied.The reactions result in formation of monocyclic pyrilium salts.

Ethynyl Carbocations. V. Synthesis and Properties of 4-Phenylethynyl-4H-pyrans

Koblik, A. V.,Murad'yan, L. A.

, p. 245 - 253 (2007/10/03)

A method for preparation of 4-phenylethynyl-4H-pyrans was developed, and their reactions with acid reagents, resulting in 4-phenylethynylpyrylium salts and 1,5-diketones containing ethynyl and allene moieties, were studied.Conditions for nucleophilic addi

The Relative Electron Donating Ability of Substituents, Determined in 2,6-Disubstituted Pyrylium Cations

Farcasiu, Dan,Sharma, Shalini

, p. 126 - 128 (2007/10/02)

Tha carbon-13 NMR spectra of a series of 2,6-disubstituted pyrylium compounds have been investigated.The chemical shift of C(4) is a measure of the charge density in that position of the ring.The variation of the chemical shift with the change of substitu

THE FORMATION OF OPEN-CHAIN CARBOXONIUM AND CARBIMMONIUM IONS AND THEIR HETEROCYCLIZATION TO PYRYLIUM AND PYRIDINIUM CATIONS

Pikus, A. L.,Feigel'man, V. M.,Mezheritskii, V. V.

, p. 2333 - 2337 (2007/10/02)

During the action of an anhydrous solution of perchloric acid in alcohol on methyl aryl ketones in ethyl orthoformate open-chain carboxonium salts (derivatives of the 1,5-diaryl-2-pentene-1,5-dione) were formed instead of the 2,6-diarylpyrylium perchlorat

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