1092390-02-7

Basic information

• Product Name: 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester
• Synonyms: 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester;1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[4-(2-naphthalenyl)phenyl]-;4,4,5,5-TetraMethyl-2-(4-(naphthalen-2-yl)phenyl)-1,3,2-dioxaborolane;4,4,5,5-tetramethyl-2-[4-(2-naphthalenyl)phenyl]-1,3,2-Dioxaborolane
• CAS NO: 1092390-02-7
• Molecular Formula: C₂₂H₂₃BO₂
• Molecular Weight: 330.23
• EINECS: 200-258-5
• Product Categories: Naphthalene;Organoborons
• Mol File: 1092390-02-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 467.0±24.0 °C(Predicted)
• Appearance: /
• Density: 1.10±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester(1092390-02-7)
• EPA Substance Registry System: 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester(1092390-02-7)

Safety Data

• Hazardous Substances Data: 1092390-02-7(Hazardous Substances Data)

Usage

General Description

The chemical 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester is a boronic acid derivative that is commonly used in organic synthesis. It is a pinacol ester, meaning it has a pinacol group attached to the boronic acid, which can increase its stability and reactivity. 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester is often used as a reagent in Suzuki-Miyaura cross-coupling reactions, which are important in the formation of carbon-carbon bonds in organic molecules. It can also be used in other types of organic reactions, such as the synthesis of biaryl compounds. 4-(Naphthalene-2-yl)phenylboronic acid pinacol ester is a versatile and important tool in the field of organic chemistry, and it plays a crucial role in the development of new pharmaceuticals, agrochemicals, and materials.

Upstream product

• 580-13-2 2-bromonaphthalene 
• 1679-18-1 4-Chlorophenylboronic acid 
• 73183-34-3 bis(pinacol)diborane 
• 5798-76-5 phenyl 4-bromobenzoate 
• 32316-92-0 naphthalene-2-boronic acid 
• 22082-98-0 2-(4-chlorophenyl)naphthalene 
• 2765-24-4 4'-nitro-2-phenylnaphthalene 
• 17763-80-3 para-nitrophenyl triflate 

Downstream Products

• 1233221-53-8 C₅₆H₃₆N₂ 

Relevant articles and documents

Functional Group Interconversion: Decarbonylative Borylation of Esters for the Synthesis of Organoboronates

A new and efficient nickel-catalyzed decarbonylative borylation reaction of carboxylic acid esters with bis(pinacolato)-diboron has been developed. This transformation allows access to structurally diverse aryl as well as alkenyl and alkyl boronate esters with high reactivity, broad substrate scope, and excellent functional-group tolerance. Further experiments show that this protocol can be carried out on a gram scale and applied to orthogonal synthetic strategies.

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE, AND DISPLAY DEVICE

The present invention is related to a first compound for an organic optoelectronic device represented by Chemical Formula 1, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device. In Chemical Formula 1, definitions of each substituent are the same as defined in the specification.

Iron-Catalyzed Borylation of Aryl Ethers via Cleavage of C-O Bonds

Herein, we report the iron-catalyzed borylation of aryl ethers and aryl amines via cleavage of C-O and C-N bonds. This protocol does not require the use of Grignard reagents and displays a broad substrate scope, which allows the late-stage borylation. It also provides facile access to multisubstituted arenes through C-H functionalization using 2-pyridyloxy as the directing group.