947770-80-1

Basic information

• Product Name: 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran
• Synonyms: 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran;B-(Dibenzofuran-2-yl)boronic acid pinacol ester;Dibenzofuran, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-;2-(dibenzo[b,d]furan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-(dibenzo[b,d]furan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(WXC08408)
• CAS NO: 947770-80-1
• Molecular Formula: C₁₈H₁₉BO₃
• Molecular Weight: 294.15266
• Mol File: 947770-80-1.mol
• Article Data: 24

Chemical Properties

• Appearance: /
• Density: 1.15
• CAS DataBase Reference: 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran(947770-80-1)
• EPA Substance Registry System: 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran(947770-80-1)

Safety Data

• Hazardous Substances Data: 947770-80-1(Hazardous Substances Data)

Usage

Description

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran, with the chemical abstracts service number 947770-80-1, is a synthetic organic compound characterized by its unique structure that incorporates a dibenzofuran core and a tetramethly-1,3,2-dioxaborolan-2-yl group. 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran is known for its potential applications in various chemical processes and industries due to its distinct chemical properties.

Uses

Used in Organic Synthesis:
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran is used as a synthetic intermediate for the development of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran is used as a key building block for the creation of novel drug molecules. Its ability to form stable intermediates and participate in complex organic reactions contributes to the development of new therapeutic agents with improved efficacy and safety profiles.
Used in Agrochemical Development:
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran also finds application in the agrochemical sector, where it is utilized in the synthesis of new pesticides and herbicides. Its chemical versatility aids in the design of more effective and environmentally friendly crop protection agents.
Used in Specialty Chemicals Production:
In the production of specialty chemicals, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran is employed as a versatile intermediate. Its unique properties enable the synthesis of a variety of high-value specialty chemicals used in industries such as materials science, fragrances, and dyes.

Upstream product

• 86-76-0 2-bromodibenzo[b,d]furan 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 3693-22-9 dibenzo[b,d]furan-2-amine 
• 73183-34-3 bis(pinacol)diborane 
• 5408-56-0 2-iododibenzofuran 
• 132-64-9 dibenzofuran 
• 51230-49-0 2-chlorodibenzofuran 
• 76-09-5 2,3-dimethyl-2,3-butane diol 

Downstream Products

• 1426925-58-7 C₂₁H₁₄N₄O 
• 955959-86-1 2-(4-bromophenyl)dibenzo[b,d]furan 
• 1246308-82-6 2-(2-nitrophenyl)dibenzo[b,d]furan 
• 1246308-85-9 12H-benzofuro[3,2-a]carbazole 

Relevant articles and documents

Organic light-emitting diode having alleviated luminance reduction in low dynamic range

The present disclosure relates to an organic light-emitting diode which can operate at a low voltage with high efficiency and exhibits the effect of having an alleviated luminance reduction rate in a low dynamic range. More particularly, the organic light-emitting diode comprises: a first electrode; a second electrode facing the first electrode; and a light-emitting layer and a charge balance control layer arranged sequentially between the first and the second electrode, wherein the light-emitting layer includes at least one of amine derivative compounds represented by the following Chemical Formula A and the charge balance control layer includes at least one of anthracene derivative compounds represented by the following Chemical Formula B or C. The structures of Chemical Formulas A, B, and C are as defined in the specification.

Visible Light-Induced Borylation of C-O, C-N, and C-X Bonds

Boronic acids are centrally important functional motifs and synthetic precursors. Visible light-induced borylation may provide access to structurally diverse boronates, but a broadly efficient photocatalytic borylation method that can effect borylation of a wide range of substrates, including strong C-O bonds, remains elusive. Herein, we report a general, metal-free visible light-induced photocatalytic borylation platform that enables borylation of electron-rich derivatives of phenols and anilines, chloroarenes, as well as other haloarenes. The reaction exhibits excellent functional group tolerance, as demonstrated by the borylation of a range of structurally complex substrates. Remarkably, the reaction is catalyzed by phenothiazine, a simple organic photocatalyst with MW 200 that mediates the previously unachievable visible light-induced single electron reduction of phenol derivatives with reduction potentials as negative as approximately - 3 V versus SCE by a proton-coupled electron transfer mechanism. Mechanistic studies point to the crucial role of the photocatalyst-base interaction.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING SAME, AND ELECTRONIC DEVICE THEREFOR

The present disclosure provides: a compound capable of providing high light-emitting efficiency, low driving voltage, and improved lifetime of a device; an organic electronic element using the same; and an electronic device therefor.