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

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

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 
• 106-40-1 4-bromo-aniline 
• 1493-27-2 ortho-nitrofluorobenzene 
• 58476-59-8 4-bromo-N-(2-nitrophenyl)benzenamine 
• 100953-52-4 N¹-(4-bromophenyl)benzene -1,2 -diamine 
• 5419-55-6 Triisopropyl borate 
• 121-43-7 Trimethyl borate 
• 7732-18-5 water 

Downstream Products

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

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