597553-98-5

Basic information

• Product Name: B-(9,10-Diphenyl-2-anthracenyl)boronic acid
• Synonyms: B-(9,10-Diphenyl-2-anthracenyl)boronic acid;9,10-diphenylanthracen-2-yl-2-boronic acid;2-boronic-9,10-diphenylanthracene;(9,10-Diphenylanthracen-2-yl)boronic acid;9,10-diphenyl-9,10-dihydroanthracene-2-boronic acid;9,10-Diphenylanthracene-2-boronic Acid (contains varying amounts of Anhydride);9,10-Diphenylanthracene-2-yl boronic acid
• CAS NO: 597553-98-5
• Molecular Formula: C₂₆H₁₉BO₂
• Molecular Weight: 374.24
• Mol File: 597553-98-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 569.6 °C at 760 mmHg
• Flash Point: 298.3 °C
• Appearance: /
• Density: 1.28
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 8.45±0.30(Predicted)
• CAS DataBase Reference: B-(9,10-Diphenyl-2-anthracenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: B-(9,10-Diphenyl-2-anthracenyl)boronic acid(597553-98-5)
• EPA Substance Registry System: B-(9,10-Diphenyl-2-anthracenyl)boronic acid(597553-98-5)

Safety Data

• Hazardous Substances Data: 597553-98-5(Hazardous Substances Data)

Usage

General Description

B-(9,10-Diphenyl-2-anthracenyl)boronic acid is a chemical compound known for its applications in fluorescent materials. Specifically, it's used as a probe in fluorescence sensing due to its exceptional photochemical stability and the ability to undergo efficient fluorescence resonance energy transfer. The compound contains boronic acid, which enables it to bind with sugar molecules and other compounds containing 1,2 or 1,3 diols, amplifying its utility in sensing applications. This chemical is typically prepared in a laboratory setting and must be handled with care due to its hazardous and irritating properties.

InChI:InChI=1S/C26H19BO2/c28-27(29)20-15-16-23-24(17-20)26(19-11-5-2-6-12-19)22-14-8-7-13-21(22)25(23)18-9-3-1-4-10-18/h1-17,28-29H

Upstream product

• 201731-79-5 2-bromo-9,10-diphenylanthracene 
• 5419-55-6 Triisopropyl borate 
• 7732-18-5 water 
• 108-86-1 bromobenzene 
• 117-79-3 2-aminoanthraquinone 
• 572-83-8 2-bromoanthracene-9,10-dione 
• 1299493-18-7 C₂₆H₂₁BrO₂ 
• 150-46-9 triethyl borate 
• 591-51-5 phenyllithium 
• 121-43-7 Trimethyl borate 

Downstream Products

• 1027074-26-5 C₃₉H₂₆N₂ 
• 1027074-45-8 C₄₀H₂₈N₂ 
• 1245526-45-7 2-(2-nitrophenyl)-9,10-diphenylanthracene 
• 1245526-46-8 6,11-diphenyl-13H-13-azaindeno[1,2-b]anthracene 
• 1245525-50-1 6,11-diphenyl-13-methyl-13-azaindeno[1,2-b]anthracene 
• 1096769-82-2 10'-(9,9-dimethyl-9H-fluoren-2-yl)-9,10-diphenyl-2,9'-bianthracene 
• 1123921-68-5 2-(4-bromophenyl)-9,10-diphenylanthracene 
• 1350928-50-5 C₆₄H₄₀ 
• 1350928-44-7 9-bromo-7,12-diphenylbenzofluoranthene 
• 1350928-56-1 C₇₀H₄₄ 

Relevant articles and documents

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

The invention provides a naphthocarbazole derivative which has a structure as shown in the formula (I), wherein Ar1-Ar12 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 Ar13 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 novel compound 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.

Light emitting compound and organic light-emitting diode including the same

PURPOSE: A light emitting compound is provided to ensure excellent luminous efficiency, power efficiency and brightness, to be used as a host material of a light-emitting layer and to increase service life of an organic electroluminescence device. CONSTITUTION: A light emitting compound is represented by chemical formula(1). In chemical formula(1), X1 - X4 are selected from the group consisting of C1-19 substituted or unsubstituted alkyl group, C1-19 substituted or unsubstituted alkoxy group, cyano group, C1-19 substituted or unsubstituted silyl group, nitro group, hydroxyl group, C1-19 substituted or unsubstituted amino group, C1-19 substituted or unsubstituted sulfonic acid group, halogen, deuterium, hydrogen C1-19 substituted or unsubstituted aryl group, heteroaryl group and heterocycle group; A1 and A2 are independently selected from the group consisting of C, N, S, O, Si and Ge; and L1 and L2 are selected from the group consisting of substituted or unsubstituted C3-40 aryl group, heteroaryl group, and heterocyclic group.

Organic EL Device

A highly stable organic EL material having the properties of both benzofluoranthene and anthracene structures is provided. The organic EL device has at least one organic compound layer containing a compound presented by the general formula (I) below: (in which L is a linking group linking any one of the positions 1 to 12 and any one of the positions 13 to 22; the unlinked positions 1 to 22 are substituted by any of a hydrogen atom, substituted or unsubstituted aryl group, substituted or unsubstituted heterocyclic group, substituted or unsubstituted alkyl group, and aromatic amino group; and L presents any of a single bond, substituted or unsubstituted arylene group, substituted or unsubstituted heterocyclic group, and substituted or unsubstituted alkylene group).