872050-52-7

Basic information

• Product Name: 4-(1-Pyrenyl)phenylboronic Acid
• Synonyms: 4-(1-Pyrenyl)phenylboronic Acid;(4-(Pyren-1-yl)phenyl)boronic acid;Boronic acid, [4-(1-pyrenyl)phenyl]-;4-(1-Pyrenyl)benzeneboronic acid;4-(1-Pyrenyl)phenylboronic Acid (contains varying amounts of Anhydride);4-(1-pyrene-yl)-phenylboronic acid;Boronic acid, B-[4-(1-pyrenyl)phenyl]-
• CAS NO: 872050-52-7
• Molecular Formula: C₂₂H₁₅BO₂
• Molecular Weight: 322.1643
• EINECS: -0
• Mol File: 872050-52-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 562.2±53.0 °C(Predicted)
• Appearance: /
• Density: 1.33±0.1 g/cm3(Predicted)
• PKA: 8.58±0.16(Predicted)
• CAS DataBase Reference: 4-(1-Pyrenyl)phenylboronic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1-Pyrenyl)phenylboronic Acid(872050-52-7)
• EPA Substance Registry System: 4-(1-Pyrenyl)phenylboronic Acid(872050-52-7)

Safety Data

• Hazardous Substances Data: 872050-52-7(Hazardous Substances Data)

Usage

General Description

4-(1-Pyrenyl)phenylboronic acid is a chemical compound that consists of a pyrene group linked to a phenylboronic acid. It is commonly used in organic synthesis and as a reagent in Suzuki coupling reactions to form carbon-carbon bonds. The boronic acid functionality makes it a useful tool for the detection and quantification of diol-containing compounds, such as sugars, through a process called boronate affinity chromatography. Additionally, its pyrene group allows for its use as a fluorescent probe in various biological and environmental applications, such as detecting the presence of specific proteins or pollutants. Overall, 4-(1-Pyrenyl)phenylboronic acid has a wide range of applications in chemical research and analysis.

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 5419-55-6 Triisopropyl borate 
• 345924-29-0 1-(4-Bromophenyl)pyrene 
• 164461-18-1 1-pyrenylboronic acid 
• 109-72-8 n-butyllithium 
• 121-43-7 Trimethyl borate 
• 349666-24-6 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene 

Downstream Products

• 386267-36-3 ethyl (2,6-dibromo-4'-pyren-1-yl-biphenyl)-4-carboxylate 
• 386267-59-0 3-bromo-4'-pyren-1-yl-biphenyl-2,5-dicarboxylic acid dimethyl ester 
• 386267-37-4 ethyl (2,6-dibromo-4'-pyren-1-yl-biphenyl-4-yl)acetate 
• 386267-40-9 [2,6-bis-(3-tert-butoxycarbonylamino-propyl)-4'-pyren-1-yl-biphenyl-4-yl]acetic acid 
• 386267-38-5 ethyl 2,6-bis-(3-tert-butoxycarbonylamino-propyl)-4'-pyren-1-yl-biphenyl-4-carboxylate 
• 386267-39-6 ethyl [2,6-bis-(3-tert-butoxycarbonylamino-propyl)-4'-pyren-1-yl-biphenyl-4-yl]acetate 
• 386267-33-0 4,4,5,5-tetramethyl-2-(4-pyren-1-yl)-phenyl-1-yl-1,3,2-dioxaborolane 

Relevant articles and documents

Pyrene structure-containing compound, and organic luminescent device thereof

The invention discloses a pyrene structure-containing compound, and an organic luminescent device thereof. The pyrene structure-containing compound is formed through combination of a pyrene ring structure with a fluorene alkenyl; on one hand, a foldable three dimensional structure is achieved, so that certain distortion of the pyrene structure-containing compound in the space three-dimensional structure is realized, and the film forming performance is improved; on the other hand, the pyrene structure possesses relatively high triplet state energy level and relatively wide energy gap, and excellent blue light performance, when the pyrene ring structure is connected with fluorene alkenyl with electron withdrawing performance, green light or red light is emitted after bathochromic shift. Thepyrene structure-containing compound possesses appropriate HOMO and LUMO values, is capable of blocking transmission from cavities to electron transmission layers, and improving effective luminescence. When the pyrene structure-containing compound is applied in organic luminescent devices, the pyrene structure-containing compound is taken as a luminescent layer or a cavity blocking layer, low driving voltage and high luminescent efficiency of the organic luminescent devices are achieved.

FLUORENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

Disclosed is a fluorene derivative having a specific structure. Also disclosed is an organic electroluminescent device having high luminous efficiency wherein an organic thin film layer composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. At least one layer of the organic thin film layer contains the fluorene derivative of the specific structure alone or as a component of a mixture. Such an organic electroluminescent device with high luminous efficiency can be realized by this fluorene derivative.