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Pyrylium, 4-methyl-2,6-diphenyl-, tetrafluoroborate(1-) is a complex organic compound with the chemical formula C17H14BF4O. It is a derivative of pyrylium, a heterocyclic compound with a six-membered ring containing one oxygen atom and five carbon atoms. In this specific compound, the 4-position of the pyrylium ring is substituted with a methyl group, while the 2 and 6 positions are occupied by phenyl groups. The tetrafluoroborate ion (BF4-) is attached to the compound, acting as a counterion. Pyrylium, 4-methyl-2,6-diphenyl-, tetrafluoroborate(1-) is of interest in organic chemistry due to its unique structure and potential applications in the synthesis of various organic compounds. It is important to note that handling and storage of Pyrylium, 4-methyl-2,6-diphenyl-, tetrafluoroborate(1-) should be done with caution, as it may have hazardous properties.

2340-23-0

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2340-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2340-23-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2340-23:
(6*2)+(5*3)+(4*4)+(3*0)+(2*2)+(1*3)=50
50 % 10 = 0
So 2340-23-0 is a valid CAS Registry Number.

2340-23-0Relevant academic research and scientific papers

A pyrylium-coumarin dyad as a colorimetric receptor for ratiometric detection of cyanide anions by two absorption bands in the visible region

Shiraishi, Yasuhiro,Nakamura, Masaya,Matsushita, Naoyuki,Hirai, Takayuki

, p. 195 - 201 (2016)

We synthesized a pyrylium-coumarin dyad (1) and used it for colorimetric detection of cyanide anions (CN-) in aqueous media. The receptor itself exhibits a long-wavelength absorption band at 643 nm due to the strong intramolecular charge transf

REACTIONS OF ACETOPHENONES AND BORON TRIFLUORIDE ETHERATE IN THE PRESENCE OF HOMOLOGS OF ORTHOFORMIC ESTER

Boiko, I. I.,Dergunova, M. E.,Boiko, T. N.

, p. 1169 - 1171 (1987)

It was established that homologs of orthoformic ester (orthoacetic and orthopropionic esters), in contrast to it, do not undergo reaction with substituted acetophenones and boron trifluoride etherate to give γ-alkylpyrylium salts; the products obtained are 2,4,6-triarylpyrylium tetrafluoroborates.

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

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

, 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

SYNTHESIS AND CHARACTERIZATION OF NEW TYPES OF 4-PYRIDINIUM BETAINE DYES

Mori, Akira,Kanemasa, Shuji,Fujimoto, Etsuo,Wada, Eiji,Takeshita, Hitoshi,et al.

, p. 869 - 878 (2007/10/02)

Two types of pyridinium betaine dyes, 4-phenolates and 2-phenolates, which have a chromophore either of ET-30 type or the stilbazolium betaine type, have been synthesized.Both types of dyes sho

THE FIRST HOMOLYTIC SUBSTITUTION OF PYRYLIUM SALTS. C-4 METHYLATION OF 2,6-DISUBSTITUTED PYRYLIUM CATIONS.

Doddi, Giancarlo,Ercolani, Gianfranco

, p. 817 - 822 (2007/10/02)

2,6-Diphenylpyrylium and 2,6-di-t-butylpyrylium cations react with methyl radical generated by ButOOH-Fe+2 in acidic aqueous acetonitrile, to yield substitution exclusively at C-4 position.

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