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3'-methyl-1'-(4-nitrophenyl)pyrazolino[60]fullerene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

690255-10-8

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690255-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 690255-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,2,5 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 690255-10:
(8*6)+(7*9)+(6*0)+(5*2)+(4*5)+(3*5)+(2*1)+(1*0)=158
158 % 10 = 8
So 690255-10-8 is a valid CAS Registry Number.

690255-10-8Relevant academic research and scientific papers

Nitration of fullerene derivatives under mild conditions

Oswald, Frederic,De La Cruz, Pilar,Langa, Fernando

, p. 1051 - 1054 (2007)

A new family of N-(2,4-dinitrophenyl)-2-pyrazolino[60]fullerene derivatives has been synthesized by electrophilic nitration using nitronium triflate. As evidenced by CV and OSWV experiments, these species show enhanced electron-accepting properties (up to

The Isoindazole Nucleus as a Donor in Fullerene-Based Dyads. Evidence for Electron Transfer

Delgado, Juan L.,De La Cruz, Pilar,Lopez-Arza, Vicente,Langa, Fernando,Kimball, David B.,Haley, Michael M.,Araki, Yasuyuki,Ito, Osamu

, p. 2661 - 2668 (2004)

A series of isoindazole-C60 dyads 4a-c based on pyrazolino[60]fullerene have been prepared by 1,3-dipolar cycloadditions of the nitrile imines, generated in situ from hydrazones 3a-c, to C60. Molecular orbital calculations for 4b revealed that the electron distribution of the HOMO is located on the isoindazole moiety, while the electron distribution of the LUMO is located on the C60 moiety. Electrochemical properties of the new dyads 4a-c show a similar electron affinity with respect to C60. Charge-transfer interactions in the ground state between the isoindazole ring and the fullerene cage are predicted by the molecular orbital calculations and confirmed by electrochemical studies in 4a,b. Steady-state fluorescence emission spectra of dyads 4a-c show that fluorescence intensities in polar benzonitrile solvent decrease with increasing electron-donating ability of the substituent attached on the isoindazole group. This was confirmed by the shortening of fluorescence lifetimes, from which intramolecular charge-separation rates and efficiencies via the excited singlet states of the fullerene moiety were evaluated. The yields of the triplet states in polar solvent decrease with the electron-donating ability, supporting the competitive formation of the charge-separated state with the intersystem crossing from the excited states. Thus, isoindazole[60]fullerene 4b can be considered a molecular switch with an AND logic gate.

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