868046-59-7

Usage

Uses

Used in Pharmaceutical Industry:
(4’-formyl-[1,1’-biphenyl]-4-yl)boronic acid is used as a synthetic intermediate for the development of pharmaceutical compounds. Its unique reactivity and ability to form reversible covalent bonds with diols make it a promising candidate for the creation of new drugs and therapeutic agents.
Used in Materials Science:
In the field of materials science, (4’-formyl-[1,1’-biphenyl]-4-yl)boronic acid is used as a building block for the synthesis of advanced materials with specific properties. Its formyl group and biphenyl structure can be exploited to create materials with tailored characteristics for various applications.
Used in Catalysis:
(4’-formyl-[1,1’-biphenyl]-4-yl)boronic acid is utilized as a catalyst or catalyst precursor in various chemical reactions. Its unique reactivity allows it to facilitate specific transformations, making it a valuable component in the development of new catalytic processes and systems.

Upstream product

• 214745-69-4 2-(4’-bromo-[1,1’-biphenyl]-4-yl)-1,3-dioxolane 
• 4612-26-4 1,4-Phenyldiboronic acid 
• 1122-91-4 4-bromo-benzaldehyde 
• 92-86-4 4-(4-bromophenyl)bromobenzene 
• 50670-58-1 4-formyl-4'-bromobiphenyl 

Downstream Products

• 1259332-56-3 C₈₈H₁₁₈O₂₁ 

Relevant academic research and scientific papers

1, 3, 5 - cyclohexanetriol - cis - or organic boronic acid-stable siloxy inositol complex and organic synthetic reaction using a reagent art

PROBLEM TO BE SOLVED: To provide a stable ate-type complex of an organoboronic acid as a reagent for organic synthesis reaction; and manufacturing techniques thereof.SOLUTION: A stable ate-type complex of an organoboronic acid with scyllo-inositol or 1,3,5-cis-cyclohexanetriol comprises an anion represented by the specified general formula (I) or (II) as a constituent. In the formula, Rand Reach represent an alkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group or aralkyl group which may have substituents.

Palladium supported on aminopropyl-functionalized polymethylsiloxane microspheres: Simple and effective catalyst for the Suzuki-Miyaura C-C coupling

Abstract A palladium catalyst, obtained in the reaction of PdCl2(MeCN)2 with microspheric aminopropyl polymethylsiloxane, was used in the Suzuki-Miyaura cross-coupling of various aryl bromides with phenylboronic acids. Catalytic reactions, performed at 80°C in a 2-propanol/water mixture, led to high yields of non-symmetric biphenyls. In recycling experiments, excellent results (up to 100%) were obtained in ten subsequent runs. Efficient separation of the catalyst from organic products was achieved by simple filtration due to the properties of microspheres.

Cyclic thiourea/urea functionalized triphenylamine-based dyes for high-performance dye-sensitized solar cells

Six cyclic thiourea/urea functionalized triphenylamine-based dyes (AZ1-AZ6) containing 2-cyanoacrylic acid as an acceptor and various linkers (phenyl, biphenyl, and bithiophene) were synthesized. They exhibited high photovoltaic performance owing to an improved short-circuit photocurrent density (J sc) and open-circuit voltage (Voc). Among them, AZ6 bearing a cyclic thiourea group and bithiophene linker showed the highest power conversion efficiency (PCE) up to 7.29%, which was comparable to that of N719 (PCE = 7.36%).

Three-dimensional four-connecting organic scaffolds with a twist: Synthesis and self-assembly

We have synthesized a novel class of four-connecting three-dimensional molecular scaffolds 2-5 based on biaryls for supramolecular self-assembly. The X-ray crystal structure analysis of 2 with ethanol reveals a novel O-H...O hydrogen-bonded helical self-a