867044-33-5

Basic information

• Product Name: [4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid
• Synonyms: 4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenylboronic acid;[4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid;[4-(2-phenyl-1H-1,3-benzodiazol-1-yl)phenyl]boronic acid;(4-(2-Phenyl-1H-benzo[d]iMidazol-1-yl)phenyl)boronic acid;Boronicacid, [4-(2-phenyl-1H-benziMidazol-1-yl)phenyl]- (9CI);[4-(2-Phenyl-1H-benziMidazol-1-yl)phenyl]boronic acid (PBIPBA;Boronic acid,B-[4-(2-phenyl-1H-benziMidazol-1-yl)phenyl]-;(4-(2-Phenyl-1H-benzo[d]imidazol-1-yl)
• CAS NO: 867044-33-5
• Molecular Formula: C₁₉H₁₅BN₂O₂
• Molecular Weight: 314.15
• Mol File: 867044-33-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 572.6 ºC at 760 mmHg
• Flash Point: 300.1 ºC
• Appearance: /
• Density: 1.21
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: [4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid(867044-33-5)
• EPA Substance Registry System: [4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid(867044-33-5)

Safety Data

• Hazardous Substances Data: 867044-33-5(Hazardous Substances Data)

Usage

Description

[4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid is a chemical compound characterized by the molecular formula C18H14BNO2. It features a boronic acid functional group, which is instrumental in a variety of organic synthesis reactions, particularly the Suzuki-Miyaura cross-coupling. [4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid is recognized for its potential in the development of pharmaceuticals, agrochemicals, and materials science due to its capacity to form stable complexes with diols, amines, and other nucleophiles. Additionally, its fluorescent properties render it a valuable component in the creation of fluorescent chemosensors for the detection of specific biological and environmental analytes.

Uses

Used in Pharmaceutical Development:
[4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid is utilized as a key intermediate in the synthesis of pharmaceuticals for its ability to form stable complexes with various biologically relevant molecules, enhancing the compound's potential therapeutic effects and selectivity.
Used in Agrochemical Synthesis:
In the agrochemical industry, [4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid is employed as a building block in the creation of new agrochemicals, leveraging its reactivity in organic synthesis to produce compounds with desired pesticidal or herbicidal properties.
Used in Materials Science:
[4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid is used as a component in the development of advanced materials, capitalizing on its capacity to form stable complexes to improve material properties such as stability, reactivity, or selectivity in various applications.
Used in Fluorescent Chemosensor Development:
[4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid is utilized as a fluorescent moiety in the design of chemosensors for detecting specific analytes in biological and environmental samples, due to its inherent fluorescent properties that can be modulated in response to target interactions.

Upstream product

• 760212-58-6 4-(2-phenyl-1H-benzo[d]imidazol-1-yl)1-bromobenzene 
• 121-43-7 Trimethyl borate 
• 7732-18-5 water 
• 5419-55-6 Triisopropyl borate 
• 100953-52-4 N¹-(4-bromophenyl)benzene -1,2 -diamine 
• 58476-59-8 4-bromo-N-(2-nitrophenyl)benzenamine 
• 1493-27-2 ortho-nitrofluorobenzene 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 944801-79-0 9-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]anthracene 

Relevant articles and documents

Compound and organic electroluminescent device

The invention provides a novel organic electroluminescent material for an organic electroluminescent device, and the organic electroluminescent device using the novel organic electroluminescent material. The novel organic electroluminescent material provi

A phenanthro imidazole symmetrical derivatives of the main material and electroluminescent device

The invention relates to a phenanthroimidazole symmetric derivative host material. The structure of the host material is represented by formula I, and can be used to form an organic electroluminescent device with the advantages of high luminescence efficiency, low driving voltage, long life, high brightness and high color purity. In the formula I, R1 and R2 are respectively independently selected from the hydrogen atom, substituted or unsubstituted C1-C30 alkyl groups, C1-C30 cycloalkyl groups, C1-C30 saturated alkyl groups, substituted or unsubstituted C1-C30 alkyloxy groups, substituted or unsubstituted C6-C30 aryl groups, substituted or unsubstituted C6-C30 aryloxy groups, substituted or unsubstituted C6-C30 arylamino groups, substituted or unsubstituted C2-C30 heterocyclic groups, substituted or unsubstituted C6-C30 fused polycyclic groups, hydroxy groups, cyan groups or substituted or unsubstituted amino groups.

Boron-containig benzopyrenes derivatives, their preparation and organic electroluminescent device (by machine translation)

The present invention relates to a 6-tritolyl-6H-6-bora benzo[cd]pyrene derivative represented by a formula (1), wherein substituents are described in an instruction. The present invention further relates to uses of the compound as an electron transportation material, and an organic electroluminescent device containing the compound. Formula (1).