108989-36-2

Usage

Uses

Used in Organic Synthesis:
3,3''-DIBROMO-4,4''-DIMETHOXYBIPHENYL is used as a building block in organic synthesis for the creation of a variety of other organic compounds. Its specific functional groups and structural features make it a valuable intermediate in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In Pharmaceutical Research, 3,3''-DIBROMO-4,4''-DIMETHOXYBIPHENYL is used as a key component in the development of new drugs. Its versatile chemical structure allows for the exploration of its potential in treating various medical conditions, making it a promising candidate for drug discovery.
Used in Agrochemical Development:
3,3''-DIBROMO-4,4''-DIMETHOXYBIPHENYL is also utilized in the agrochemical industry as a precursor for the synthesis of new pesticides or other agrochemicals. Its reactivity and structural attributes can contribute to the development of effective and environmentally friendly products.
Used as a Reagent in Chemical Reactions:
In the context of chemical reactions, 3,3''-DIBROMO-4,4''-DIMETHOXYBIPHENYL serves as a reagent, facilitating specific transformations or providing a pathway for the synthesis of desired products.
Used as a Reference Compound in Analytical Testing:
3,3''-DIBROMO-4,4''-DIMETHOXYBIPHENYL is used as a reference compound in analytical testing to ensure the accuracy and reliability of experimental results. Its well-defined chemical properties make it suitable for comparison and calibration purposes in various analytical techniques.

Upstream product

• 2132-80-1 4,4'-Dimethoxybiphenyl 
• 578-57-4 2-bromoanisole 

Downstream Products

• 1415582-03-4 C₂₆H₂₁BrO₂ 
• 1415581-94-0 C₃₂H₂₆O₂ 
• 1415582-01-2 C₃₂H₂₆O₂ 
• 1415581-80-4 C₂₈H₂₀F₆O₂ 
• 1415581-81-5 C₂₈H₂₆O₄ 
• 1415581-82-6 C₂₄H₂₀N₂O₂ 
• 1415581-83-7 C₃₀H₃₀O₆ 
• 1415581-84-8 C₂₈H₂₂O₄ 
• 1415581-85-9 C₃₈H₃₀O₂ 
• 1608458-34-9 C₂₆H₂₄Cl₂O₆ 
• 1608458-09-8 C₂₆H₂₈Cl₂O₆ 
• 1608457-99-3 C₂₈H₃₂Cl₂O₄ 

Relevant academic research and scientific papers

Regioselective halogenation of biphenyls for preparation of valuable polyhydroxylated biphenyls and diquinones

Electron-rich biphenyls were selectively oxyfunctionalised through a halogenation-methoxylation sequence. The obtained biphenyl methyl ethers were then oxidised to the corresponding quinones. This strategy transforms commercially available biphenyls into both natural and bioactive oxidised compounds.

Efficient oxidative biaryl coupling reaction of phenol ether derivatives using hypervalent iodine(III) reagents

Oxidative biaryl coupling reaction of phenol ether derivatives with the hypervalent iodine reagent, phenyliodine(III) bis(trifluoroacetate) (PIFA), in the presence of BF3·Et2O gave a variety of substituted biphenyl and binaphthyl compounds in high yields. Replacement of PIFA with a more practical polymer-supported hypervalent iodine reagent has also been achieved.

Synthesis of polyphenyls

A facile synthetic route toward functionalized 3-aryl-, 3,3′-diaryl-, 3,3′,5-triaryl-4,4′-dimethoxybiphenyls (polyphenyls) 3-5 with the terphenyl, quaterphenyl, quinquephenyl, and sexiphenyl skeleton starting from biphenyl-4,4′-diol (1) in modest total yield is described. The route has been carried by the two transformations of the regioselective NBS (N-bromosuccinimide)-mediated bromination of 2 in MeCN at reflux and Suzuki-Miyaura cross-coupling reaction of the resulting bromides with arylboronic acids 6 in DME at reflux.