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2,5-Bis(methoxymethyl)-1,4-dimethoxybenzene is an organic compound with the molecular formula C11H16O4. It is a colorless, crystalline solid that is soluble in organic solvents. 2,5-Bis(methoxymethyl)-1,4-dimethoxybenzene is characterized by its symmetrical structure, featuring two methoxymethyl groups attached to the 2 and 5 positions of a benzene ring, with two additional methoxy groups at the 1 and 4 positions. It is synthesized through the reaction of 1,4-dimethoxybenzene with paraformaldehyde in the presence of a base, such as potassium carbonate. 2,5-Bis(methoxymethyl)-1,4-dimethoxybenzene is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and as a precursor in the preparation of polymers. Its stability and reactivity make it a valuable building block in organic chemistry.

5628-37-5

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5628-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5628-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5628-37:
(6*5)+(5*6)+(4*2)+(3*8)+(2*3)+(1*7)=105
105 % 10 = 5
So 5628-37-5 is a valid CAS Registry Number.

5628-37-5Relevant academic research and scientific papers

ELECTROCHEMICALLY ACTIVE AGENTS FOR PH MODULATION IN BIOLOGICAL BUFFERS

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Paragraph 00301, (2017/01/26)

Device and methods for use in a biosensor comprising a multisite array of test sites, the device and methods being useful for modulating the binding interactions between a (biomolecular) probe or detection agent and an analyte of interest by modulating the pH or ionic gradient near the electrodes in such biosensor. An electrochemically active agent comprising quinone derivatives that is suitable for use in biological buffers for changing the pH of the biological buffers. Method for changing the pH of biological buffers using the electrochemically active agents. The methods of modulating the binding interactions provided in a biosensor, analytic methods for more accurately controlling and measuring the pH or ionic gradient near the electrodes in such biosensor, and analytic methods for more accurately measuring an analyte of interest in a biological sample.

Radical-Cation Catalysis in the Synthesis of Diphenylmethanes via the Dealkylative Coupling of Benzylic Ethers

Rathore, Rajendra,Kochi, Jay K.

, p. 7479 - 7490 (2007/10/03)

The dealkylative coupling of benzyl alkyl ethers (ArCH2OR) to yield the corresponding diarylmethanes (ArCH2Ar) together with dialkoxymethane (ROCH2OR) is catalyzed by small amounts of 1-electron oxidants (such as aromatic cation radicals, NO(1+), etc.) or by an equivalent electrochemical (anodic) method.The catalytic method is successfully employed for the facile synthesis of a novel macrocyclic crown ether 18 that contains a diarylmethane linkage.On the basis of the spectral observation of the radical cation ArCH2OR.+ and the excellent catalytic efficiency with turnover numbers in excess of 1E2, an electron-transfer and an alternative electrophilic chain mechanism are discussed for the dealkylative coupling process.

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