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(Z)-3-(2-oxo-2-phenylethylidene)-7-chloro-3,4-dihydroquinoxalin-2-one is a complex organic compound with a molecular formula of C16H11ClN2O2. It is a derivative of quinoxaline-2-one, featuring a 7-chloro substitution and a (Z)-3-(2-oxo-2-phenylethylidene) group. (Z)-3-(2-oxo-2-phenylethylidene)-7-chloro-3,4-dihydroquinoxalin-2-one is characterized by its unique structure, which includes a quinoxaline core with a double bond between the 2 and 3 positions, a phenyl group attached to the 2 position, and a chlorine atom at the 7 position. The compound is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or materials science due to its specific structural features.

34029-99-7

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34029-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34029-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34029-99:
(7*3)+(6*4)+(5*0)+(4*2)+(3*9)+(2*9)+(1*9)=107
107 % 10 = 7
So 34029-99-7 is a valid CAS Registry Number.

34029-99-7Downstream Products

34029-99-7Relevant academic research and scientific papers

The effect of substituents on the response of 3,4-dihydro-3-(2-oxo-2- phenylethylidene)-quinoxalin-2(1H)-one derivatives toward binding of Cu 2+

Korin, Efrat,Cohen, Beny,Bai, Yue-Xia,Zeng, Cheng-Chu,Becker, James Y.

, p. 7450 - 7455 (2012)

A new series of fluorogenic chelating reagents based on phenylethylidene-3,4-dihydro-1H-quinoxalin-2-one with different substituents (attached either to the quinoxaline-2-one (3) or phenyl ring (4)) have been investigated to examine the effect of the substituent (nature/position) on the spectral properties and response toward Cu2+ in the presence of other metal cations, in ethanol. It was found that all of the examined ligands exhibit a pronounced response to Cu2+ addition resulting in a red-shift in the UV-vis spectra and a strong quenching in the fluorescence spectra. Among the ligands examined, 3a exhibits the highest selectivity toward various metal cations. In general it appears that the best response selectivity of these ligands toward Cu2+ ion is obtained by either EDG in 3 or EWG in 4. For example, the fluorescence intensity of 3a (with OMe substituent) increases to about three times that of the unsubstituted derivative.

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