1056113-50-8

Basic information

• Product Name: 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-dibenzofuran
• Synonyms: 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-dibenzofuran;(dibenzofuran-3-yl)boronic acid pinacol ester;2-(dibenzo[b,d]furan-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(WXC08407)
• CAS NO: 1056113-50-8
• Molecular Formula: C₁₈H₁₉BO₃
• Molecular Weight: 294.15266
• EINECS: -0
• Mol File: 1056113-50-8.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-dibenzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-dibenzofuran(1056113-50-8)
• EPA Substance Registry System: 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-dibenzofuran(1056113-50-8)

Safety Data

• Hazardous Substances Data: 1056113-50-8(Hazardous Substances Data)

Usage

General Description

3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-dibenzofuran is a chemical compound that belongs to the family of boron-containing compounds. It is a dibenzofuran derivative that contains a boron atom attached to a tetramethyl dioxaborolan group. 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-dibenzofuran has potential applications in organic synthesis and material science due to its unique boron and furan functionalities. It may be used as a reagent in organic reactions or as a building block for the synthesis of more complex molecules. Its specific properties and potential uses make it a target for further research and development in various fields of chemistry.

Upstream product

• 3693-22-9 dibenzo[b,d]furan-2-amine 
• 96042-30-7 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 
• 132-64-9 dibenzofuran 
• 5410-97-9 3-nitrodibenzofuran 
• 4106-66-5 3-aminodibenzofuran 
• 26608-06-0 3-bromodibenzofuran 
• 73183-34-3 bis(pinacol)diborane 
• 120612-68-2 diazotiertes 2-Amino-diphenylenoxyd 
• 40981-28-0 dibenzo[b,d]furan-3-yl-dimethyl-amine 

Downstream Products

• 2142681-84-1 2-chloro-4-(dibenzo[b,d]furan-3-yl)-6-phenyl-1,3,5-triazine 

Relevant articles and documents

Unreactive C-N Bond Activation of Anilines via Photoinduced Aerobic Borylation

Unreactive C-N bond activation of anilines was achieved by photoinduced aerobic borylation. A diverse range of tertiary and secondary anilines were converted to aryl boronate esters in moderate to good yields with wide functional group tolerance under simple and ambient photochemical conditions. This transformation achieved the direct and facile C-N bond activation of unreactive anilines, providing a convenient and practical route transforming widely available anilines into useful aryl boronate esters.

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE, AND DISPLAY DEVICE

The present invention is related to a first compound for an organic optoelectronic device represented by Chemical Formula 1, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device. In Chemical Formula 1, definitions of each substituent are the same as defined in the specification.

Organic compound based on triazine and anthrone structure, and applications thereof

The invention relates to an organic compound based on a triazine and anthrone structure, and applications in OLED devices. The compound has high glass transition temperature and high molecular thermalstability, and is low in absorption in the field of vis