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(3,4-dimethoxy-phenyl)-(4-methoxy-phenyl)-methane, also known as 1,1'-(1-methylethylidene)bis(2,5-dimethoxybenzene), is an organic compound with the molecular formula C17H20O4. It is a symmetrical molecule consisting of two 3,4-dimethoxyphenyl groups connected by a methane bridge. (3,4-dimethoxy-phenyl)-(4-methoxy-phenyl)-methane is characterized by its aromatic structure, with each phenyl ring containing two methoxy substituents, which contribute to its polarity and solubility properties. It is often used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound is typically synthesized through the condensation of 3,4-dimethoxybenzaldehyde with acetone in the presence of an acid catalyst. Its chemical properties, such as its ability to undergo electrophilic aromatic substitution, make it a valuable intermediate in organic chemistry.

2898-55-7

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2898-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2898-55-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2898-55:
(6*2)+(5*8)+(4*9)+(3*8)+(2*5)+(1*5)=127
127 % 10 = 7
So 2898-55-7 is a valid CAS Registry Number.

2898-55-7Downstream Products

2898-55-7Relevant academic research and scientific papers

Proton-exchanged montmorillonite-mediated reactions of methoxybenzyl esters and ethers

Chen, Dongyin,Xu, Chang,Deng, Jie,Jiang, Chunhuan,Wen, Xiaoan,Kong, Lingyi,Zhang, Ji,Sun, Hongbin

, p. 1975 - 1983 (2014/03/21)

Proton-exchanged montmorillonite (H-mont) was found to be an eco-friendly and cost-effective catalyst for the generation of O-methylated quinone methides (QM) from the corresponding p or o-methoxybenzyl esters and ethers. Nucleophilic trapping of the O-methylated QM with arenes, alcohols, 1,3-dicarbonyl compounds, silyl enol ethers, and allylsilanes has been carried out, respectively, leading to eco-friendly benzylation reactions. Using this protocol, H-mont-mediated deprotection of PMB-protected esters and ethers have been realized for the first time. This work would pave the way for further exploration in O-alkylated QM that are of chemical and biological significance.

Iodine-catalyzed disproportionation of aryl-substituted ethers under solvent-free reaction conditions

Jereb, Marjan,Vrazic, Dejan

, p. 1978 - 1999 (2013/05/22)

Iodine was demonstrated to be an efficient catalyst for disproportionation of aryl-substituted ethers under solvent-free reaction conditions. Variously substituted 1,1,1′,1′-tetraaryldimethyl ethers were transformed into the corresponding diarylketone and diarylmethane derivatives. I 2-catalyzed transformation of 4-methoxyphenyl substituted ethers yielded mono- and dialkylated Friedel-Crafts products as well. Treatment of trityl alkyl and trityl benzyl ethers with a catalytic amount of iodine produced triphenylmethane and the corresponding aldehydes and ketones. The electron-donating substituents facilitated the reaction, while the electron-withdrawing groups retarded it; the difference in reactivity is not very high. Such an observation may be in favour of hydride transfer, predominantly from the less electron rich side of the ether with more stable carbocation formation. With the isotopic studies it was established that a substantial portion of the C-H bond scission took place in the rate-determining step, while the carbonyl oxygen atom originated from the starting ether, and not from the air. The transformation took place under air and under argon, and HI was not a functioning catalyst.

Br?nsted acid-catalyzed synthesis of diarylmethanes under non-genotoxic conditions

Mendoza, Oscar,Rossey, Guy,Ghosez, Léon

experimental part, p. 2235 - 2239 (2011/05/05)

Triflic acid and triflimide were found to efficiently catalyze the formation of a wide diversity of diarylmethanes from the non-genotoxic benzylic acetates and electron-rich arenes or heteroarenes. The reaction worked best with acetates capable of generating a stabilized benzylic cationic species. In most cases, the reactions were conveniently run in the absence of solvent under mild conditions.

One-step synthesis of diphenylmethanes

Wei, Qiyan,Luo, Yinggang,Zhou, Min,Tao, Feiyan,Zhang, Guoling

, p. 835 - 843 (2007/10/03)

The coupling reaction of substituted toluenes themselves and the cross-coupling reaction of substituted toluene and aromatic in the presence of bromine in anhydrous CC14 under irradiation lead to diphenylmethanes with moderate to good yields. The methylen

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