1219637-88-3

Basic information

• Product Name: 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
• Synonyms: 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
• CAS NO: 1219637-88-3
• Molecular Weight: 293.173
• Mol File: 1219637-88-3.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 474.3±18.0 °C(Predicted)
• Density: 1.16±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(1219637-88-3)
• EPA Substance Registry System: 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(1219637-88-3)

Safety Data

• Hazardous Substances Data: 1219637-88-3(Hazardous Substances Data)

Usage

Description

1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is a chemical compound characterized by the presence of a boron atom within a dioxaborolane group attached to a carbazole ring. This unique structure, which includes a five-membered ring with two oxygen atoms and one boron atom, endows the compound with specific reactivity and utility in organic chemistry.

Uses

Used in Organic Synthesis:
1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is utilized as a reagent in organic synthesis, particularly for selective cross-coupling reactions. Its distinctive structure and reactivity allow for the efficient formation of carbon-carbon bonds, even in the presence of other functional groups, making it a valuable tool in this field.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole may be employed as a building block for the development of novel therapeutic agents. Its ability to form stable carbon-carbon bonds can be leveraged in the synthesis of complex molecular structures with potential medicinal applications.
Used in Material Science:
1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole can also be used in material science for the creation of new materials with specific properties. 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole's capacity to form carbon-carbon bonds can contribute to the development of advanced polymers, composites, or other materials with tailored characteristics for various applications.

Upstream product

• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 10294-33-4 boron tribromide 
• 19264-68-7 9-benzoyl-9H-carbazole 
• 70950-05-9 1-(9H-carbazol-9-yl)-2,2-dimethylpropan-1-one 
• 86-74-8 9H-carbazole 
• 5599-70-2 1-chlorocarbazole 
• 73183-34-3 bis(pinacol)diborane 
• 16807-11-7 1-bromo-9H-carbazole 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Relevant articles and documents

A procedure for transforming indoles into indolequinones

A procedure that converts a series of structurally diverse, readily available indole derivatives to their corresponding indolequinones is described. The three-step route commences with an iridium catalyzed C-H borylation to give a 7-borylindole that upon

Color-Tunable Solid-State Fluorescence Emission from Carbazole-Based BODIPYs

Several carbazole-based boron dipyrromethene (BODIPY) dyes were synthesized by organometallic approaches. Thiazole, benzothiazole, imidazole, benzimidazole, triazole, and indolone substituents were introduced at the 1-position of the carbazole moiety, and boron complexation of each dipyrrin generated the corresponding compounds 1, 2 a, and 3-6. The properties of these products were investigated by UV/Vis and fluorescence spectroscopy, cyclic voltammetry, X-ray crystallography, and DFT calculations. These compounds exhibited large Stokes shifts, and compounds 1, 2 a, and 3-5 fluoresced both in solution and in the solid state. Complex 2 a showed the highest fluorescence quantum yield (ΦF) in the solid state, therefore boron complexes of the carbazole-benzothiazole hybrids 2 b-f, which had several different substituents, were prepared and the effects of the substituents on the photophysical properties of the compounds were examined. The fluorescence properties showed good correlation with the results of crystal-packing analyses, and the dyes exhibited color-tunable solid-state fluorescence.

Nitrogen-containing compound, organic electroluminescent element, and electronic device

The invention belongs to the technical field of organic materials, and provides a nitrogen-containing compound, an organic electroluminescent device and an electronic device. The structure of the nitrogen-containing compound is as shown in formula 1, and the nitrogen-containing compound can improve the performance of the organic electroluminescent device.

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present specification relates to a compound of Formula 1 and an organic light emitting device including the same.