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2,5-Dimethoxy-1,4-bis-(2,5-dimethoxy-4-methyl-benzyl)-benzol is a complex organic compound with the molecular formula C26H30O6. It is characterized by a central benzene ring (C6H6) with two methoxy groups (-OCH3) attached at the 2nd and 5th positions. Each of the 1st and 4th positions on the benzene ring is connected to a benzyl group, which itself contains a 2,5-dimethoxy-4-methyl-benzene structure. 2,5-Dimethoxy-1,4-bis-(2,5-dimethoxy-4-methyl-benzyl)-benzol is known for its potential applications in the synthesis of certain pharmaceuticals and as a precursor in the production of other organic compounds. Its structure provides it with unique chemical properties, making it a subject of interest in organic chemistry research.

3753-72-8

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3753-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3753-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3753-72:
(6*3)+(5*7)+(4*5)+(3*3)+(2*7)+(1*2)=98
98 % 10 = 8
So 3753-72-8 is a valid CAS Registry Number.

3753-72-8Downstream Products

3753-72-8Relevant academic research and scientific papers

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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