1126522-69-7

Basic information

• Product Name: 9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
• Synonyms: 9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole;9-Phenyl-9H-carbazole-3-boronic acid pinacol ester;9-phenyl-9H-carbazol-3-yl-3-boronic acid pinacol ester;9-phenyl-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole (PCBAPE);3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (9-phenyl-9H-carbazol-3-yl)boronate;9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole;9-Phenyl-3-
• CAS NO: 1126522-69-7
• Molecular Formula: C₂₄H₂₄BNO₂
• Molecular Weight: 369.26386
• Mol File: 1126522-69-7.mol
• Article Data: 51

Chemical Properties

• Melting Point: 162.0 to 166.0 °C
• Boiling Point: 478.328 °C at 760 mmHg
• Flash Point: 243.084 °C
• Appearance: /
• Density: 1.11
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Solubility: soluble in Toluene
• CAS DataBase Reference: 9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(1126522-69-7)
• EPA Substance Registry System: 9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(1126522-69-7)

Safety Data

• Hazardous Substances Data: 1126522-69-7(Hazardous Substances Data)

Usage

Chemical Properties

Pale yellow powder

Upstream product

• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 1150-62-5 N-phenylcarbazole 
• 13517-10-7 boron triiodide 
• 108-86-1 bromobenzene 
• 1592-95-6 3-bromo-9H-carbazole 
• 343864-78-8 4-bromo-2-iodo-1-nitrobenzene 
• 98-80-6 phenylboronic acid 
• 105971-15-1 5-bromo-2-nitro-biphenyl 
• 73183-34-3 bis(pinacol)diborane 
• 502161-03-7 3-iodo-9-phenyl-9H-carbazole 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 591-50-4 iodobenzene 
• 1153-85-1 3-bromo-9-phenyl-9H-carbazole 
• 86-74-8 9H-carbazole 

Downstream Products

• 1150-62-5 N-phenylcarbazole 
• 1060735-14-9 9-phenyl-3,3'-bicarbazole 
• 1340668-15-6 9-(dibenzo[b,d]thiophen-2-yl)-9'-phenyl-9H,9'H-3,3'-bicarbazole 
• 1345143-20-5 9-(dibenzo[b,d]thiophen-4-yl)-9?-phenyl-9H,9'H-3,3?-bicarbazole 
• 1345143-16-9 C₄₂H₂₆N₂O 
• 1345143-22-7 C₄₁H₂₅N₃S 
• 1345970-18-4 C₄₁H₂₅N₃O 
• 1314320-92-7 3-(anthracen-9-yl)-9-phenyl-9H-carbazole 
• 1268622-33-8 diphenyl-[4'-(9'-phenyl-9H,9'H-[3,3']bicarbazolyl-9-yl)biphenyl-4-yl]amine 
• 1384321-94-1 9-phenyl-3-(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-9Hcarbazole 
• 1984-49-2 9H,9′H-[3,3′]bicarbazole 
• 1346668-29-8 C₄₇H₃₁N₃ 
• 1345202-03-0 9’-phenyl-2,3’-bi-9H-carbazole 
• 1346668-97-0 C₄₇H₃₁N₃ 

Relevant articles and documents

Thermally activated delayed fluorescence of N-phenylcarbazole and triphenylamine functionalised tris(aryl)triazines

N-phenyl carbazole and triphenylamine functionalized tris(aryl)triazines, as well as the corresponding mononers, have been synthesized by Suzuki cross-coupling reactions. The electronic, photophysical and electrochemical properties of these materials can be effectively tuned by manipulation of the constitution of acceptor and donor units. N-phenyl carbazole and triphenylamine functionalized 2,4,6-trisphenyl-1,3,5-triazines exhibit small energy gaps between the singlet and triplet (0.24 eV and 0.18 eV), and offer potential for application as thermally activated delayed fluorescence materials. The results are supported by time-dependent density functional theory calculations, delayed and time-resolved fluorescence data.

Thiophene ethylene malononitrile structural compound and preparation method thereof

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Multiple Electrophilic C-H Borylation of Arenes Using Boron Triiodide

Electrophilic C-H borylation of arenes using boron triiodide has been developed. This reaction proceeded smoothly in the absence of additives, and the diiodoboryl group was installed at the most sterically accessible carbon, where the HOMO is localized to a certain extent. Moreover, regioselective multiple borylation of polycyclic aromatic compounds was achieved by using excess boron triiodide. The borylated intermediates were transformed into a variety of arylboron compounds such as arylboronates, boronic acids, and trifluoroborates.