269410-05-1

Basic information

• Product Name: 2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-Methoxy-1-naphthaleneboronic acid pinacol ester
• CAS NO: 269410-05-1
• Molecular Formula: C17H21BO3
• Molecular Weight: 284.15784
• Mol File: 269410-05-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 419.5±28.0 °C(Predicted)
• Appearance: /
• Density: 1.08±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(269410-05-1)
• EPA Substance Registry System: 2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(269410-05-1)

Safety Data

• Hazardous Substances Data: 269410-05-1(Hazardous Substances Data)

Usage

Description

2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a complex organic compound that serves as a key intermediate in the synthesis of various organic molecules, particularly those with potential applications in the field of organic electronics.

Uses

Used in Organic Electronics Industry:
2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a synthetic intermediate for the preparation of substituted Dibenzonaphthodifurans and their analogs. These compounds are electroactive and have potential applications in the manufacturing of organic electronic devices, such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The compound's unique structure allows for the creation of novel materials with improved electronic properties, contributing to the advancement of organic electronic technologies.

Upstream product

• 32721-21-4 1-iodo-2-methoxynapthalene 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 
• 3401-47-6 1-bromo-2-methoxynaphthalene 
• 573-97-7 1-bromo-2-naphthol 
• 135-19-3 β-naphthol 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 75640-87-8 (S)-2,2'-dimethoxy-1,1'-dinaphthyl 

Relevant articles and documents

Economical and Readily Accessible Preparation of o,o-Disubstituted Arylboronates through Palladium-Catalyzed Borylation of Haloarenes

Miyaura borylation, that is, palladium-catalyzed cross-coupling between bromoarenes and diboron, offers a versatile method for preparing arylboronates; however, a costly and inaccessible catalyst has been required for synthesizing highly congested arylboronates with the method. Here the Pd(OAc)2–tri(4-methoxyphenyl)phosphine catalyst was found to work as an efficient catalyst for the sterically demanding borylation. A broad range of o,o-disubstituted bromoarenes were converted into the corresponding arylboronates in high yields by using the palladium catalyst with Cs2CO3 in EtOAc at 80 °C.

NOVEL COMPOUND, PHOTOACID GENERATOR CONTAINING THE COMPOUND, AND PHOTOSENSITIVE RESIN COMPOSITION CONTAINING THE PHOTOACID GENERATOR

PROBLEM TO BE SOLVED: To provide a nonionic photoacid generator with high acid generation quantum yield. SOLUTION: The present invention provides a compound represented by formula (2) (where, ring Ar is a benzene ring, naphthalene ring, thiophene ring or

ORGANIC COMPOUND AND ORGANIC OPTOELECTRIC DEVICE AND DISPLAY DEVICE

The present invention relates to an organic compound represented by chemical formula 1, an organic optoelectronic device including the organic compound, and a display device. In chemical formula 1, X is O, S, CRaRb or SiRcRd; and Y is N or CRe, wherein at least one Y is N; Ar1 is a substituted or unsubstituted fused ring; Ra to Rd are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C3 to C12 cycloalkyl group, a substituted or unsubstituted C6 to C12 aryl group, a substituted or unsubstituted C3 to C12 heterocyclic group, or a combination thereof; and Re is hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heterocyclic group, or a combination thereof.COPYRIGHT KIPO 2016