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CALIX(4)HYDROQUINONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125583-08-6

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125583-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125583-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,8 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125583-08:
(8*1)+(7*2)+(6*5)+(5*5)+(4*8)+(3*3)+(2*0)+(1*8)=126
126 % 10 = 6
So 125583-08-6 is a valid CAS Registry Number.

125583-08-6Downstream Products

125583-08-6Relevant academic research and scientific papers

Mechanistic Study on Electrochemical Reduction of Calix[4]quinone in Acetonitrile Containing Water

Kim, Young-Ok,Jung, Young Mee,Kim, Seung Bin,Hong, Byung Hee,Kim, Kwang S.,Park, Su-Moon

, p. 4927 - 4936 (2007/10/03)

The mechanism of electrochemical reduction of calix[4]quinones (CQs) is of vital importance, as their reduction products, calix[4]hydroquinones (CQH 8s), are known to self-assemble organic nanotubes, which in turn self-assemble novel metal nanostructures by a self-synthetic process of electrochemical reduction of solvated metals. We therefore conducted detailed studies of electrochemical reduction of CQ in rigorously dried acetonitrile (CH3CN) and in CH3CN containing varied amounts of water as well as perchloric acid. CQ undergoes a series of reversible one electron reductions in dry CH3CN leading to anion radicals of each of p-benzoquinone units followed by formation of dianions. However, a series of following chemical-electrochemical reactions with protons takes place after the initial electron transfer in CH3CN containing water. The final product of this series of reactions is identified as CQH8 via an eight electron, eight proton reaction. The intermediate species are identified, and the reaction mechanism is elucidated using transient electrochemical, electrochemical quartz crystal microbalance and spectroelectrochemical measurements. The present results could be utilized to fine control the self-assembling reaction of nanotubes by electrochemical processes and to design electrochemically controllable nanomechanical devices.

Syntheses and NMR Behavior of Calixquinone and Calixhydroquinone

Morita, Yutaka,Agawa, Toshio,Nomura, Eisaku,Taniguchi, Hisaji

, p. 3658 - 3662 (2007/10/02)

Calixquinone (7) and calixhydroquinone (6) have been synthesized using three different synthetic pathways.The first pathway to 7 from calixarene (1) consists of six steps: acetylation, Fries rearrangement, Baeyer-Villiger oxidation after acetylat

Syntheses and Crystal Structure of Calixquinone

Morita, Yutaka,Agawa, Toshio,Kai, Yasushi,Kanehisa, Nobuko,Kasai, Nobutami,et al.

, p. 1349 - 1352 (2007/10/02)

Calixquinone and other functionalized calixarenes were synthesized in high yields.The crystal structure of the calixquinone was determined by the X-ray diffraction method.

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