Description

4-(1-Phenyl-1H-Benzimidazol-2-Yl)Phenylboronic Acid is a high-value, functionalized boronic acid derivative that serves as a critical building block in modern synthetic chemistry. Its unique structure, combining a benzimidazole core with a boronic acid functional group, makes it an essential reagent for constructing complex molecules via cross-coupling reactions. This compound is primarily sought after by research institutions and pharmaceutical companies engaged in the development of new active pharmaceutical ingredients (APIs), advanced materials, and specialty chemicals. Its precise synthesis and high purity are paramount for ensuring successful downstream applications and reproducible results.

Application

• Pharmaceutical Intermediate: A key precursor in Suzuki-Miyaura cross-coupling reactions for synthesizing novel drug candidates, particularly those targeting complex heterocyclic structures.
• Organic Light-Emitting Diode (OLED) Materials: Used in the research and development of advanced organic electronic materials for display and lighting technologies.
• Ligand Synthesis for Catalysis: Serves as a building block for creating sophisticated ligands used in transition metal catalysis.
• Polymer Chemistry: Incorporated into specialty polymers to impart specific electronic or binding properties.
• Chemical Biology Probes: Utilized in the design of molecular probes for studying biological processes and target identification.
• Academic & Industrial R&D: A versatile reagent for methodological development and exploratory synthesis in both academic and industrial research laboratories.

Basic Information

Product Name	4-(1-Phenyl-1H-Benzimidazol-2-Yl)Phenylboronic Acid
CAS No.	952514-79-3
Molecular Formula	C19H15BN2O2
Molecular Weight	314.15 g/mol
Synonyms	[4-(1-Phenylbenzimidazol-2-yl)phenyl]boronic acid; 2-[4-(Boronophenyl)]-1-phenyl-1H-benzimidazole; 4-(1-Phenyl-1H-benzo[d]imidazol-2-yl)benzeneboronic acid; 4-(1-Phenylbenzimidazol-2-yl)phenylboronic acid; 4-(1-Phenyl-1H-benzimidazol-2-yl)phenylboronic acid; B-[4-(1-Phenyl-1H-benzimidazol-2-yl)phenyl]boronic acid
EINECS	Contact for details

Quality Control

Our production of 4-(1-Phenyl-1H-Benzimidazol-2-Yl)Phenylboronic Acid adheres to stringent quality management protocols to ensure batch-to-batch consistency and high purity. Each lot is subjected to comprehensive analytical testing, including HPLC for purity determination, NMR for structural confirmation, and elemental analysis. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting all critical quality attributes. We support cGMP-compliant manufacturing for pharmaceutical applications upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which can affect stability and reactivity. For long-term storage, consider using desiccants or storing under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 1.0%
Heavy Metals	≤ 20 ppm
Residue on Ignition	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.