654664-63-8

Basic information

• Product Name: B-2-Triphenylenylboronic acid
• Synonyms: B-2-Triphenylenylboronic acid;Triphenylen-2-ylboronic acid;9,10-BenzophenanthreN-2-ylboronicacid;triphenylene-2-yl boronic acid;Triphenylen-2-ylboronic acid/ B-2-Triphenylenylboronic acid;Boronic acid, B-2-triphenylenyl-;Boronic acid, 2-triphenylenyl-;2-Triphenylenylboronic acid
• CAS NO: 654664-63-8
• Molecular Formula: C₁₈H₁₃BO₂
• Molecular Weight: 272.10562
• Product Categories: OLED materials,pharm chemical,electronic
• Mol File: 654664-63-8.mol

Chemical Properties

• Boiling Point: 565.5±33.0 °C(Predicted)
• Appearance: /
• Density: 1.30
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.53±0.30(Predicted)
• CAS DataBase Reference: B-2-Triphenylenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: B-2-Triphenylenylboronic acid(654664-63-8)
• EPA Substance Registry System: B-2-Triphenylenylboronic acid(654664-63-8)

Safety Data

• Hazardous Substances Data: 654664-63-8(Hazardous Substances Data)

Usage

Chemical Properties

Yellow solid

Upstream product

• 121-43-7 Trimethyl borate 
• 19111-87-6 2-bromobenzo[9,10]phenanthrene 
• 217-59-4 triphenylene 
• 5419-55-6 Triisopropyl borate 

Downstream Products

• 1158227-53-2 C₅₄H₃₄ 
• 1313400-54-2 9-phenyl-3-[3-(2-triphenylenyl)phenyl]-9H-carbazole 
• 1158227-56-5 2-(4-bromophenyl)triphenylene 

Relevant articles and documents

A phenanthro carbazole derivatives and their use in the organic electroluminescent device in the application of the

The invention provides a phenanthrocarbazole derivative which has a structure as shown in the formula (I), wherein Ar1-Ar8 are independently selected from one of H, C6-C30 substituted or unsubstituted aromatic group, C6-C30 substituted or unsubstituted fused ring aromatic group, C6-C30 substituted or unsubstituted fused heterocyclic group, pentabasic and hexabasic heterocyclic ring or substituted heterocyclic ring, triarylated amine group, arylether group and C1-C12 substituted or unsubstituted aliphatic alkyl group; and Ar9 is selected from one of C6-C30 substituted or unsubstituted aromatic group, C6-C30 substituted or unsubstituted fused ring aromatic group and C1-C12 substituted or unsubstituted aliphatic alkyl group. The phenanthrocarbazole derivative can be used as a hole-injection material, a hole-transmission material, a fluorescence host material or a luminescent material in an organic electroluminescence device.

ORGANIC LIGHT EMITTING DEVICE AND DISPLAY DEVICE HAVING THE SAME

An organic light emitting device and a display device including the same, the organic light emitting device including a first electrode; a hole controlling layer on the first electrode; an emission layer on the hole controlling layer; an electron controlling layer on the emission layer; and a second electrode on the electron controlling layer, wherein the emission layer includes a hole transport host material, an electron transport host material, a bipolar host material, and at least one dopant material.

Compound, material for organic electroluminescent elements, organic electroluminescent element and electronic device

Provided are a high performance organic electroluminescent element and an electronic device which is provided with this organic electroluminescent element. Also provided is a compound which enables the achievement of the organic electroluminescent element and the electronic device. Specifically provided are: a compound of a specific structure having a triphenylene skeleton; an organic electroluminescent element which uses this compound; and an electronic device which is provided with this organic electroluminescent element.

Compound, material for organic electroluminescent elements, organic electroluminescent element and electronic device

Provided are: an organic electroluminescent element which exhibits higher performance and has particularly good driving voltage and external quantum efficiency, while having a longer service life; and an electronic device which is provided with this organic electroluminescent element. Also provided is a compound which enables the achievement of the organic electroluminescent element and the electronic device. Specifically provided are: a compound of a specific structure having a triphenylene skeleton; an organic electroluminescent element which uses this compound; and an electronic device which is provided with this organic electroluminescent element.

NOVEL ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME

Organic electroluminescent compounds comprising a triphenylene conjugated to a five-ring fused heterocyclic system, as depicted in formula 1 are provided. Also provided is an organic electroluminescent device comprising these compounds. The organic electroluminescent compounds disclosed herein exhibit good luminous efficiency and excellent material life. They can be used to manufacture OLED devices very superior in terms of operating life and which consume less power due to improved power efficiency.

BLUE ELECTROLUMINESCENT COMPOUNDS WITH HIGH EFFICIENCY AND DISPLAY DEVICE USING THE SAME

The present invention relates to novel organic electroluminescent compounds and display devices comprising the same. The organic electroluminescent compounds according to the present invention exhibit high luminous efficiency and excellent life property, so that an OLED device having very good operation life can be prepared therefrom.