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4,4'-Stilbenequinone is an organic compound with the chemical formula C14H8O2. It is a derivative of stilbene, featuring a quinone functional group, which consists of two carbonyl groups (C=O) attached to the same carbon atom. This molecule is characterized by its conjugated double bonds and aromatic rings, which contribute to its unique electronic properties and chemical reactivity. 4,4'-Stilbenequinone is known for its potential applications in the synthesis of various organic compounds and materials, such as polymers and dyes. It is also of interest in the field of organic chemistry due to its ability to participate in redox reactions and its potential use as a building block for more complex molecules.

3457-53-2

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3457-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3457-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3457-53:
(6*3)+(5*4)+(4*5)+(3*7)+(2*5)+(1*3)=92
92 % 10 = 2
So 3457-53-2 is a valid CAS Registry Number.

3457-53-2Downstream Products

3457-53-2Relevant academic research and scientific papers

A joint experimental and theoretical investigation on the oxidative coupling of resveratrol induced by copper and iron ions

Tamboli, Vajir F.,Re, Nazzareno,Coletti, Cecilia,Defant, Andrea,Mancini, Ines,Tosi, Paolo

, p. 55 - 63 (2012)

Currently, a mounting interest exists on the biological activity of polyphenolic compounds, which have been suggested to exert positive effects on the human health. In this paper we report the first electrospray ionization mass spectrometry (ESI-MS) study on the gas-phase production of isomeric δ-viniferin and ε-viniferin dimers in racemic form, starting from acetonitrile/water solutions containing resveratrol and CuSO4 or FeCl3, respectively. Interestingly, the formation of racemic δ-viniferin dehydrodimer is observed in ESI-MS experiments carried out on resveratrol-copper mixtures, while the analogous resveratrol-iron reaction affords the racemic ε-viniferin dehydrodimer. The use of gas-phase techniques and of ab initio calculations, at BHandHLYP/LACV3P + +** level of theory, allowed us to elucidate some important aspects of these reaction mechanisms. In particular, a different stability for the resveratrol radicals involved in the oxidative coupling has been obtained in the presence of copper ion, favoring the formation of δ-viniferin, as proposed for the in vivo mechanism where copper is able to switch the resveratrol from an antioxidant to a prooxidant agent. Finally, the structure-reactivity relationship has been investigated for synthetic analogues of resveratrol, showing the crucial role of the OH group in para position.

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