155079-10-0

Basic information

• Product Name: 2-PHENYLPYRIDINE-5-BORONIC ACID
• Synonyms: 5-Borono-2-phenylpyridine;2-PHENYL-5-PYRIDINYL-5-BORONIC ACID;2-PHENYLPYRIDINE-5-BORONIC ACID;6-PHENYLPYRIDINE-3-BORONIC ACID;(6-PHENYLPYRIDIN-3-YL)BORONIC ACID;Boronic acid, B-(6-phenyl-3-pyridinyl)-
• CAS NO: 155079-10-0
• Molecular Formula: C₁₁H₁₀BNO₂
• Molecular Weight: 199.01
• Mol File: 155079-10-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 401.1 °C at 760 mmHg
• Flash Point: 196.4 °C
• Appearance: /
• Density: 1.24 g/cm³
• Vapor Pressure: 3.73E-07mmHg at 25°C
• Refractive Index: 1.614
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-PHENYLPYRIDINE-5-BORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYLPYRIDINE-5-BORONIC ACID(155079-10-0)
• EPA Substance Registry System: 2-PHENYLPYRIDINE-5-BORONIC ACID(155079-10-0)

Safety Data

• Hazardous Substances Data: 155079-10-0(Hazardous Substances Data)

Usage

General Description

2-Phenylpyridine-5-boronic Acid is a chemical compound typically used in the world of organic synthesis due to its ability to act as a catalyst or a reagent for various reactions. 2-PHENYLPYRIDINE-5-BORONIC ACID belongs to the boronic acid category and is characterized by the presence of a boron atom. It has significant utility in coupling reactions, specifically Suzuki-Miyauri cross-coupling reactions which are highly useful in the synthesis of complex organic compounds. The presence of the boron atom allows it to covalently bond with other organic molecules to yield new substances. As a result, 2-Phenylpyridine-5-boronic Acid is widely used in pharmaceuticals and agrochemical fields.

InChI:InChI=1/C11H10BNO2/c14-12(15)10-6-7-11(13-8-10)9-4-2-1-3-5-9/h1-8,14-15H

Upstream product

• 5419-55-6 Triisopropyl borate 
• 27012-25-5 5-bromo-2-phenylpyridine 
• 150-46-9 triethyl borate 
• 7732-18-5 water 
• 624-28-2 2,5-dibromopyridine 
• 98-80-6 phenylboronic acid 

Downstream Products

• 1268250-89-0 4,6-diphenyl-2-[5-(9-phenanthryl)-1-(6-phenylpyridin-3-yl)phenyl-3-yl]-1,3,5-triazine 
• 1257879-55-2 C₄₂H₂₆N₂ 
• 1334590-10-1 1,2,4,5-tetrakis(2-phenylpyridin-5-yl)benzene 
• 1393479-18-9 2-phenyl-5-(2,2,2-trifluoroethyl)pyridine 
• 1251041-69-6 5-(2-nitrophenyl)-2-phenylpyridine 

Relevant articles and documents

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention provides a compound of chemical formula 1 and an organic light emitting device including the same. In the chemical formula 1, at least one of R1 to R3 is a substituted or unsubstituted cycloalkyl group, and X is O or S. The compound

Bipyridyl derivative and application thereof

The present invention provides a novel compound, which has a structure general formula represented by a formula (I), wherein Ar1 and Ar2 are independently selected from an aromatic hydrocarbon derivative group containing benzimidazoyl, an aromatic hydrocarbon derivative group containing a pyridine group, substituted or unsubstituted C6-C30 aromatic hydrocarbon, and a substituted or unsubstituted C6-C30 fused ring aromatic hydrocarbon group, and R1 and R2 are independently and respectively selected from H, C1-C12 aliphatic hydrocarbon radical, phenyl, substituted phenyl, naphthyl, substituted naphthyl, biphenyl and substituted biphenyl. According to the present invention, the compound has characteristics of stable character, simple preparation process, high luminous efficiency and high carrier mobility, and can be used for the electron transport layer of the electroluminescent element, and the device applying the compound has characteristics of significant driving voltage reducing and current efficiency improving. The formula (I) is defined in the instruction.

METAL COMPLEX, POLYMER, AND ELEMENT OBTAINED USING SAME

A metal complex represented by the following formula (1) : wherein R1 to R6, R8 and R11 to R20 represent a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an alkylthio group, an aryl group, an aryloxy group, an arylthio group, an arylalkyl group, an arylalkoxy group, an arylalkylthio group, an acyl group, an acyloxy group, an amide group, an acid imide group, an imine residue, a substituted amino group, a substituted silyl group, a substituted silyloxy group, a substituted silylthio group, a substituted silylamino group, a monovalent heterocyclic group, a heteroaryloxy group, a heteroarylthio group, an arylalkenyl group, an arylalkynyl group, a substituted carboxyl group or a cyano group; Z1 to Z5 represent -C(R*)= or a nitrogen atom, wherein R* represents a hydrogen atom or a substituent, provided that at least two of Z1 to Z5 are nitrogen atoms; m represents 1 or 2.