406482-72-2

Usage

Uses

Used in Organic Synthesis:
4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl-4-carbonitrile is used as a building block for the synthesis of various organic compounds due to its unique structure and reactivity. It serves as a key intermediate in the creation of novel materials and pharmaceuticals, enhancing the diversity of chemical products.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl-4-carbonitrile is used as a starting material for the development of new drugs. Its versatility allows for the exploration of different chemical pathways and the synthesis of potential therapeutic agents.
Used in Material Science:
4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl-4-carbonitrile is utilized in material science as a component in the design and synthesis of advanced materials. Its structural features contribute to the properties of these materials, making it instrumental in the development of new technologies and applications.
Used in Chemical Research:
In the field of chemical research, 4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl-4-carbonitrile is employed as a versatile reagent for studying various chemical reactions and mechanisms. Its unique boron-containing group provides a platform for investigating new methods of functionalization and manipulation in organic chemistry.

Upstream product

• 171364-82-2 4-cyanophenylboronic acid pinacol ester 
• 5467-74-3 4-Bromophenylboronic acid 
• 3058-39-7 4-iodobenzonitrile 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 106-37-6 1.4-dibromobenzene 

Downstream Products

• 19812-93-2 4-Cyano-4'-hydroxybiphenyl 
• 406482-73-3 (4'-cyano-[1,1'-biphenyl]-4-yl)boronic acid 

Relevant academic research and scientific papers

Molecular Graph Paper

We present a self-assembled template that consists of tetraphenylmethane derivatives and adopts a periodic lateral arrangement on a Au(111) surface with acetyl groups sticking out of the molecular film. By using the tip of a scanning tunneling microscope, these acetyl groups can be removed in a spatially controlled way without significantly affecting the remaining molecular assembly. The chemically modified molecules can be readily distinguished from the original ones such that information can be engraved in the molecular film. Both the modified nature of an individual molecule and the order of the molecular film are shown to persist at room temperature. The mesh size of this molecular graph paper can be tuned by varying the length of the molecular spacer so that writing and reading information on the nanoscale with variable letter sizes becomes possible.

Electron transport material, organic electro-luminescent device and display device

The invention discloses an electron transport material shown as a general formula I, which can be used as an electron transport layer of an organic light-emitting device in a display device. The electron transport material provided by the invention has a

Compound, electron transport material, organic electroluminescent device and display device

The present application provides a compound of general formula (I), which can be used in electron transport materials. The compound has a parent structure of benzene cyano substituted naphthalene terpyridyl, has high bond energy between atoms, has good th

A synthetic approach to dimetalated arenes using flow microreactors and the switchable application to chemoselective cross-coupling reactions

In spite of their potential utility, the chemistry of dimetalated arenes is still in its infancy because they are extremely difficult to synthesize. We report a novel method of synthesizing arenes bearing a boryl group and a metallic substituent, such as boryl, silyl, stannyl, or zincyl groups, in an integrated flow microreactor based on the generation and reactions of aryllithiums bearing a trialkyl borate moiety. The bimetallic arenes showed a remarkable chemoselectivity in palladium-catalyzed cross-coupling reactions. The selectivity was switched by the selection of the metal species that constitutes the dimetalated arenes as well as appropriate catalysts.

Fluorescent chemosensors of carbohydrate triols exhibiting TICT emissions

4-4′-Disubstituted biphenyl boronic acids (BBAs) are push-pull fluorophores with "turn-on" fluorescence properties. Upon carbohydrate triol binding, BBA boronate esters can participate in photon-induced electron transfer, giving a twisted intramolecular charge transfer (TICT) complex. The resulting TICT emissions distinguish between carbohydrates that bind to boron as a diol versus triol unit, thereby revealing stereochemical information about the carbohydrate.

A modular synthesis of functionalised phenols enabled by controlled boron speciation

A modular synthesis of functionalised biaryl phenols from two boronic acid derivatives has been developed via one-pot Suzuki-Miyaura cross-coupling, chemoselective control of boron solution speciation to generate a reactive boronic ester in situ, and oxidation. The utility of this method has been further demonstrated by application in the synthesis of drug molecules and components of organic electronics, as well as within iterative cross-coupling.