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Bis-(5-chloro-2-methoxy-phenyl)-methane, also known as 4,4'-(methanediyl)bis(2-methoxy-5-chlorophenol), is an organic compound with the chemical formula C15H14Cl2O2. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. bis-(5-chloro-2-methoxy-phenyl)-methane is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its chemical structure, it exhibits properties such as stability and reactivity, which make it a valuable component in the development of these products.

7569-57-5

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7569-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7569-57-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,6 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7569-57:
(6*7)+(5*5)+(4*6)+(3*9)+(2*5)+(1*7)=135
135 % 10 = 5
So 7569-57-5 is a valid CAS Registry Number.

7569-57-5Relevant academic research and scientific papers

Functional Ionic Liquids as Efficient and Recyclable Catalysts for the Methylation of Formaldehyde with Aromatics

Song, Heyuan,Jin, Fuxiang,Jin, Ronghua,Kang, Meirong,Li, Zhen,Chen, Jing

, p. 1264 - 1272 (2016)

Abstract: Methylation of formaldehyde with various aromatics under functional ionic liquids catalysis has been developed. Among the ionic liquids investigated, triphenyl-(4-sulfobutyl)-phosphonium triflate ([TTPBs][CF3SO3]) showed high activity and afforded excellent yields of diarylmethane derivatives. A mechanism for the catalytic performance of [TTPBs][CF3SO3] is proposed. Besides, the catalyst can simply be separated from the reaction mixture by centrifugation and be recycled ten times without noticeable loss of activity. Graphical Abstract: Diarylmethane derivatives were successfully synthesized from the methylation of formaldehyde with aromatics using efficient and recyclable functional ionic liquids as catalysts, excellent yields and selectivities were obtained under solvent free conditions. The catalyst was reused at least ten consecutive recycles without noticeable loss in its catalytic activity. Meanwhile, the usability of catalyst was explored.[Figure not available: see fulltext.]

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