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Usage

Uses

Used in Organic Synthesis:
1,1'-Biphenyl,2,2',4,4'-tetramethoxyis utilized as a building block in organic synthesis for creating more complex molecules. Its presence in the synthesis process is crucial for the development of advanced chemical compounds with specific properties.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,1'-Biphenyl,2,2',4,4'-tetramethoxyis used as a key intermediate in the production of various drugs. Its unique structure allows for the creation of pharmaceuticals with targeted therapeutic effects.
Used in Agrochemicals:
1,1'-Biphenyl,2,2',4,4'-tetramethoxyis employed in the agrochemical industry as a component in the development of pesticides and other agricultural chemicals. Its properties contribute to the effectiveness and selectivity of these products.
Used in Materials Science:
In the field of materials science, 1,1'-Biphenyl,2,2',4,4'-tetramethoxyis used to develop new materials with specific characteristics. Its integration into material compositions can enhance properties such as stability, reactivity, or conductivity.
Used in Biological Research:
1,1'-Biphenyl,2,2',4,4'-tetramethoxyis studied for its potential biological activities, including its antioxidant and anti-inflammatory properties. It is used as a subject of research to explore its effects on biological systems and its potential as a therapeutic agent.

Upstream product

• 109384-40-9 (2,4-dimethoxyphenyl)zinc chloride 
• 590-17-0 cyanomethyl bromide 
• 36896-61-4 2,4-dimethoxyphenyllead triacetate 
• 17715-69-4 1-Bromo-2,4-dimethoxybenzene 
• 552-16-9 ortho-nitrobenzoic acid 
• 91-52-1 2,4 dimethoxybenzoic acid 
• 113793-83-2 2-(2-acetoxyethyl)-6-iodobenzoic acid methyl ester 
• 113793-82-1 5-(benzyloxy)-4-iodo-1,3-benzodioxole 

Downstream Products

• 4371-31-7 sappanin 
• 43042-33-7 4,4'-Dimethoxybiphenyl-2,5,2',5'-bis-p-benzoquinone 
• 35065-24-8 dibenzofuran-3,7-diol 

Relevant academic research and scientific papers

Synthesis of biaryls by Pd-catalyzed decarboxylative homo- and heterocoupling of substituted benzoic acids

By carefully choosing the right substrate ratio, catalyst combination, and base, symmetrical and unsymmetrical biaryls can be readily synthesized through the Pd-catalyzed decarboxylative homo- and heterocoupling of substituted benzoic acids. The reaction gave the desired products in 40-90% yield and is compatible with 2-nitro-, 2-methoxy-, 2-fluoro-, and 2-chloro-substituted benzoic acids. With the correct substrate ratio, catalyst combination, and base, symmetrical and unsymmetrical biaryls can be readily synthesized through the Pd-catalyzed decarboxylative homo- and heterocoupling of substituted benzoic acids.

Thieme journal awardees - Where are they now? on cobalt-catalyzed biaryl coupling reactions

An operationally simple biaryl coupling reaction has been developed. The underlying domino process involves in situ Grignard formation from aryl bromides and subsequent homocoupling with catalytic CoCl2 and 1 bar synthetic air as terminal oxidant. Georg Thieme Verlag Stuttgart.

Palladium-catalyzed cross-coupling of organolead compounds with hypervalent iodonium salts

The palladium-catalyzed cross-coupling of hypervalent iodonium salts with organolead triacetates was achieved with Pd2(dba)3 · CHCl3 (5 mol %) in the presence of NaOMe (2 equiv) in CHCl3 at room temperature.

Preparation of 7-oxaaporphine derivatives and evaluation of their dopaminergic activity

A series of 7-oxaaporphine derivatives was prepared. The compounds were evaluated as dopaminergic agents. None of them showed either affinity for dopamine receptors or activity in vivo in the climbing behavior (mice) and turning behavior (6-hydroxydopamin

Nickel-Catalyzed Synthesis of Arylacetonitriles from Arylzinc Chlorides and Bromoacetonitrile

Arylacetonitriles are synthesised by coupling arylzinc chlorides with bromoacetonitrile using Ni(acac)2/P(c-C6H11)(C6H5)2 as catalyst.The arylacetonitriles are reduced in situ with LiAlH4/AlCl3 to give the corresponding 2-aryl-1-aminoethanes.