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

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

Uses

Used in Pharmaceutical Industry:
2-Phenylpyridine-5-boronic Acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its role in coupling reactions enables the creation of complex molecules that can be further developed into potential drug candidates, contributing to the advancement of new treatments and therapies.
Used in Agrochemical Industry:
2-Phenylpyridine-5-boronic Acid is used as a building block in the development of agrochemicals, such as pesticides and herbicides. Its involvement in the synthesis of complex organic molecules allows for the creation of novel compounds with improved efficacy and selectivity, ultimately benefiting agricultural practices and crop protection.
Used in Organic Synthesis:
2-Phenylpyridine-5-boronic Acid is used as a catalyst or reagent in various organic synthesis reactions. Its ability to covalently bond with other organic molecules makes it a valuable component in the construction of complex organic structures, which can be further utilized in the development of new materials, chemicals, and compounds.

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

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

Downstream Products

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

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

ORGANOMETALLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING SAME

The present invention provides an organometallic compound represented by chemical formula 1 and an organic light emitting device including the same. In chemical formula 1, X is NR, O, S or Se, X1 is N or CRa, X2 is N or CRb, X3 is N or CRc, and X4 is N or CRd. When the organometallic compound according to the present invention is used in a light emitting layer, a device can emit bright green light.COPYRIGHT KIPO 2020

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 as well as preparation method thereof and application thereof in organic light-emitting devices

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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.