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951628-16-3

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951628-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 951628-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,6,2 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 951628-16:
(8*9)+(7*5)+(6*1)+(5*6)+(4*2)+(3*8)+(2*1)+(1*6)=183
183 % 10 = 3
So 951628-16-3 is a valid CAS Registry Number.

951628-16-3Downstream Products

951628-16-3Relevant articles and documents

Boron-Containing Polycyclic Aromatic Hydrocarbons: Facile Synthesis of Stable, Redox-Active Luminophores

Hertz, Valentin M.,Bolte, Michael,Lerner, Hans-Wolfram,Wagner, Matthias

, p. 8800 - 8804 (2015)

Herein we show that replacing the two meso carbon atoms of the polycyclic aromatic hydrocarbon (PAH) bisanthene by boron atoms transforms a near-infrared dye into an efficient blue luminophore. This observation impressively illustrates the impact of boron doping on the frontier orbitals of PAHs. To take full advantage of this tool for the targeted design of organic electronic materials, the underlying structure-property relationships need to be further elucidated. We therefore developed a modular synthesis sequence based on a Peterson olefination, a stilbene-type photocyclization, and an Si-B exchange reaction to substantially broaden the palette of accessible polycyclic aromatic organoboranes and to permit a direct comparison with their PAH congeners.

Mixed er-NHC/phosphine Pd(ii) complexes and their catalytic activity in the Buchwald-Hartwig reaction under solvent-free conditions

Ageshina, Alexandra A.,Sterligov, Grigorii K.,Rzhevskiy, Sergey A.,Topchiy, Maxim A.,Chesnokov, Gleb A.,Gribanov, Pavel S.,Nechaev, Mikhail S.,Asachenko, Andrey F.,Bermeshev, Maxim V.,Melnikova, Elizaveta K.

, p. 3447 - 3452 (2019/04/30)

A series of novel (NHC)PdCl2-PR3 complexes were synthesized and fully characterized by 1H, 13C, 31P NMR and FT-IR spectroscopy. These complexes showed high catalytic activity toward solvent-free Buchwald-Hartwig amination. Both primary and secondary amines were efficiently utilized under the same reaction conditions. The solvent-free synthesis of valuable N-aryl carbazoles and similar N-heterocyclic systems was described.

Synthesis and characterization of teranthene: A singlet biradical polycyclic aromatic hydrocarbon having kekule structures

Konishi, Akihito,Hirao, Yasukazu,Nakano, Masayoshi,Shimizu, Akihiro,Botek, Edith,Champagne, Benoit,Shiomi, Daisuke,Sato, Kazunobu,Takui, Takeji,Matsumoto, Kouzou,Kurata, Hiroyuki,Kubo, Takashi

supporting information; experimental part, p. 11021 - 11023 (2010/09/17)

A teranthene derivative has been successfully isolated in a crystalline form for the first time. Geometrical considerations and physical property investigations indicate that the molecule possesses prominent biradical character in the ground state.

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