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

Uses

Used in Pharmaceutical Industry:
(10-Phenylanthracen-9-yl)boronic acid is used as a pharmaceutical intermediate due to its ability to be incorporated into the synthesis of various drugs. Its unique chemical structure allows for the development of new therapeutic agents with potential applications in treating different medical conditions.
Used in Organic Synthesis:
(10-Phenylanthracen-9-yl)boronic acid is utilized in the Suzuki reaction, a widely used method in organic chemistry for the formation of carbon-carbon bonds. This reaction is particularly important in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials.
Used in OLED Industry:
(10-Phenylanthracen-9-yl)boronic acid is also used as a material in the development of organic light-emitting diodes (OLEDs). Its properties make it suitable for use in the creation of efficient and high-quality OLED devices, which are increasingly being used in various display technologies, such as televisions, smartphones, and other electronic devices.

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

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

Downstream Products

• 1604840-44-9 7,7-dimethyl-5-phenyl-2-(10-phenylanthracen-9-yl)-5,7-dihydroindeno [2,1-b]carbazole 
• 1604840-86-9 C₄₄H₂₇NS 
• 294881-19-9 9-(4'-bromo-[1,1'-biphenyl]-4-yl)-10-phenylanthracene 

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.

Asymmetric antracene derivatives having two phenyl groups and organic light-emitting diode including the same

The present invention relates to an antracene derivative represented by [Chemical Formula A] and an organic light-emitting diode including the same, wherein substituents X_1 to X_5, Y, and Z are the same as defined in the detailed description of the invention. [Chemical Formula A].

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.

Anthracene derivatives and organic light-emitting diode including the same

PURPOSE: An anthracene derivative is provided to have excellent power efficiency by low voltage operation and to provide an organic electroluminescent device with excellent luminance efficiency and a long lifetime. CONSTITUTION: An anthracene derivative is represented by chemical formula 1. An organic electroluminescent device includes an anode(20); a cathode(80) opposite to the anode; and an organic layer inserted between the anode and the cathode. The organic layer is one or more layers. The organic layer includes the anthracene derivative. The organic layer includes one or more layers selected from a light emitting layer(50), a hole injection layer(30), a hole transport layer(40), a hole blocking layer, an electron transport layer(60), an electron injection layer(70), and an electron blocking layer.

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.

Compound using anthracene and phenanthrene as core and application thereof to organic electroluminescence device

The invention relates to a compound using anthracene and phenanthrene as a core and application thereof to an organic electroluminescence device. The compound uses the anthracene as the core; the structural general formula is shown as a formula in the description. The characteristics of difficult crystallization between molecules, difficult aggregation and good film forming performance are realized. When the compound is used as a material of the organic electroluminescence device, the current efficiency, the power efficiency and the external quantum efficiency of the device are greatly improved; meanwhile, the obvious effect is achieved on the service life prolonging of the device.

Anthracene derivatives and organic light emitting devices comprising the same

An anthracene derivative represented by Formula 1 is disclosed. An organic light-emitting device including an anode, a cathode, and an organic layer between the anode and the cathode, where the organic layer includes at least one anthracene derivative represented by Formula 1, is also disclosed. A method of manufacturing the organic light-emitting device is also disclosed.

Organic light emitting compound and organic light emitting device including the same

Disclosed is an organic light emitting compound represented by Formula I: Also disclosed is an organic light emitting device including the organic light emitting compound. The organic light emitting device can be driven at a low voltage to achieve high power efficiency. In addition, the organic light emitting device has excellent luminescent properties, such as high luminance and high luminous efficiency. Due to these advantages, the organic light emitting device can be utilized as a display device or a lighting device.

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

An anthracene derivative represented by the following [Chemical Formula A] and an organic light emitting device including the same are provided X. 1 To X7 , Y and Z are as defined by the description of the invention. [Formula A] (by machine translation)

aromatic compound having fused cyclic substituent in aromatic ring and organic light-emitting diode including the same

The present invention relates to a compound having a cyclic substituent fused with a cyclic ring and an organic light emitting diode including the same, and more particularly, to a compound for an organic light emitting diode represented by chemical formula A and an organic light emitting diode including the same. In chemical formula A, X is a substituent having structural formula X, Y is a substituent of structural formula Y1, n is an integer from 1 to 4, and structural formulas X and Y1 are the same as described in detailed description of the present invention.