334658-75-2

Basic information

• Product Name: (10-Phenylanthracen-9-yl)boronic acid
• Synonyms: 10-phenylantrhacen-9-yl boronic acid;(10-Phenylanthracen-9-yl)boronic acid;(10-Phenylanthracen-;9-phenylanthracen-10-yl-10-boronic acid;10-Phenylanthracene-9-boronic acid;9-Borono-10-phenylanthracene;10-Phenyl-9-anthracene boronic acid;(10-Phenylanthracen-9-yl)boronic
• CAS NO: 334658-75-2
• Molecular Formula: C20H15BO2
• Molecular Weight: 298.14
• Product Categories: organic chemicals and derivatives/others;OLED;OLED materials,pharm chemical,electronic
• Mol File: 334658-75-2.mol
• Article Data: 26

Chemical Properties

• Boiling Point: 521.325 °C at 760 mmHg
• Flash Point: 269.088 °C
• Appearance: /Solid
• Density: 1.27
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.727
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: Soluble in methanol.
• PKA: 8.59±0.30(Predicted)
• Sensitive: Light Sensitive
• CAS DataBase Reference: (10-Phenylanthracen-9-yl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (10-Phenylanthracen-9-yl)boronic acid(334658-75-2)
• EPA Substance Registry System: (10-Phenylanthracen-9-yl)boronic acid(334658-75-2)

Safety Data

• Hazardous Substances Data: 334658-75-2(Hazardous Substances Data)

Usage

Chemical Properties

white powder

Uses

Different sources of media describe the Uses of 334658-75-2 differently. You can refer to the following data:
1. It is used as pharmaceutical intermediate and as OLED materials.
2. suzuki reaction

InChI:InChI=1/C20H15BO2/c22-21(23)20-17-12-6-4-10-15(17)19(14-8-2-1-3-9-14)16-11-5-7-13-18(16)20/h1-13,22-23H

Upstream product

• 5419-55-6 Triisopropyl borate 
• 23674-20-6 9-bromo-10-phenylanthracene 
• 7732-18-5 water 
• 150-46-9 triethyl borate 
• 121-43-7 Trimethyl borate 
• 108-86-1 bromobenzene 
• 100622-34-2 anthracene-9-boronic acid 
• 602-55-1 9-phenylanthracene 
• 1564-64-3 9-Bromoanthracene 
• 98-80-6 phenylboronic acid 

Downstream Products

• 1048422-33-8 diphenyl-[4-(10-phenyl-anthracene-9-yl)-phenyl]amine 

Relevant articles and documents

Dianthracene compound containing pyridyl at tail end and application thereof

The invention provides dianthracene compounds shown in a general formula I in the specification. In the general formula I, L1 and L2 independently represent single bonds, substituted or unsubstituted heterocyclic aromatic groups of C2-C60 or substituted or unsubstituted hydrocarbon aromatic groups of C6-C60; L3 represents a substituted or unsubstituted heterocyclic aromatic group of C2-C60 or a substituted or unsubstituted hydrocarbon aromatic group of C6-C60; R10, R11, R12, R13, R14, R15, R16, R17, R18, R21, R23, R24, R25, R26, R27 and R28 independently represent hydrogen, halogen and substituted or unsubstituted alkyl or alkoxy of C1-C10. The compounds have good luminescence properties, high electron transport capacities and terrific solubility and can be used in luminescent materials, electron transport materials and hole-blocking materials in the electroluminescence field. The invention also provides an organic electroluminescence device at least comprising a pair of electrodes and organic luminescent media between the electrodes. The organic luminescent media at least comprise the dianthracene compounds.

Pyrene derivatives having substituted groups and organic light-emitting diode including the same

The present invention relates to a novel compound and an organic electroluminescent device comprising the same as luminous substances, and more specifically, to a novel compound represented by formula A or formula B and an organic electroluminescent device comprising the same.

Antracene derivatives having heteroaryl substituted naphthyl group and organic light-emitting diode including the same

The present invention relates to an antracene derivative represented by the following [Formula A] and an organic light-emitting diode including the same. Substituents X_1 to X_7 , Y, and L are the same as defined in the detailed description of the invention.