400607-47-8

Basic information

• Product Name: Boronic acid, (10-[1,1'-biphenyl]-4-yl-9-anthracenyl)-
• Synonyms: Boronic acid, (10-[1,1'-biphenyl]-4-yl-9-anthracenyl)-;(10-[1,1'-Biphenyl]-4-yl-9-anthracenyl)boronic acid;B-(10-[1,1'-Biphenyl]-4-yl-9-anthracenyl)boronic acid;(10-([1,1'-Biphenyl]-4-yl)anthracen-9-yl)boronic acid;10-(4-biphenyl)anthracene-9-ylboronic acid
• CAS NO: 400607-47-8
• Molecular Formula: C26H19BO2
• Molecular Weight: 374.23886
• Mol File: 400607-47-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 623℃
• Flash Point: 331℃
• Appearance: /
• Density: 1.28
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8?+-.0.30(Predicted)
• CAS DataBase Reference: Boronic acid, (10-[1,1'-biphenyl]-4-yl-9-anthracenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Boronic acid, (10-[1,1'-biphenyl]-4-yl-9-anthracenyl)-(400607-47-8)
• EPA Substance Registry System: Boronic acid, (10-[1,1'-biphenyl]-4-yl-9-anthracenyl)-(400607-47-8)

Safety Data

• Hazardous Substances Data: 400607-47-8(Hazardous Substances Data)

Usage

Chemical Properties

light yellow powder

Upstream product

• 400607-05-8 9‐{[1,1'‐biphenyl]‐4‐yl}‐10‐bromoanthracene 

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.

NEW ANTHRACENE DERIVATIVES, PREPARATION METHOD THEREOF AND ORGANIC LIGHT EMITTING DIODE USING THE SAME

The present invention provides a novel anthracene derivative, a method for preparing the same, and an organic electronic device using the same. The anthracene derivative according to the invention can function alone as a light emitting host, in particular, as a blue host in an organic electronic device. Further, the anthracene derivative according to the invention can also function as a hole injecting or hole transporting material, an electron injecting or electron transporting material, or a light emitting material in an organic electronic device including a light emitting device. Therefore, the organic electronic device according to the present invention shows excellent characteristics in efficiency, drive voltage and stability.