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Phenol, 4-(diphenylmethyl)-2-methoxy-, also known as 2-methoxy-4-benzhydrylphenol or 4-benzhydryl-2-methoxyphenol, is an organic compound with the chemical formula C20H18O2. It is a derivative of phenol, characterized by the presence of a diphenylmethyl group (a benzene ring with two phenyl groups attached to a central carbon) at the 4-position and a methoxy group (an oxygen atom bonded to a methyl group) at the 2-position. Phenol, 4-(diphenylmethyl)-2-methoxy- is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its antioxidant properties and is sometimes used as a stabilizer in polymers. The compound is typically synthesized through the reaction of 2-methoxyphenol with benzene in the presence of a Friedel-Crafts catalyst.

848-52-2

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848-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848-52-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 848-52:
(5*8)+(4*4)+(3*8)+(2*5)+(1*2)=92
92 % 10 = 2
So 848-52-2 is a valid CAS Registry Number.

848-52-2Downstream Products

848-52-2Relevant academic research and scientific papers

Transition-Metal-Free Arylation and Alkylation of Diarylmethyl p-Tolyl Sulfones with Zinc Reagents

Miao, Maozhong,Yin, Wenguang,Wang, Lei,Chen, Zhengkai,Xu, Jianfeng,Ren, Hongjun

, p. 10602 - 10612 (2018/09/06)

The transition-metal-free synthesis of unsymmetrical and highly functionalized triarylmethanes through arylation of the situ generated o-QMs from diarylmethyl p-tolyl sulfones with aryl zinc reagents is described. Alkyl zinc reagents are also well tolerated in this reaction. Additionally, the straightforward synthesis of the analogue of the antituberculosis agent A and the key precursor of the anti-breast-cancer agent B are achieved by this strategy.

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