4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid
98%, containing different amounts of acid anhydride
Reagent
Code: #90368
CAS Number
867044-33-5
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Molecular Information
Weight
314.15 g/mol
Formula
C₁₉H₁₅BN₂O₂
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Registry Numbers
MDL Number
MFCD11977298
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of complex organic molecules. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes. Its benzimidazole moiety also contributes to its use in designing compounds with potential biological activity, such as antimicrobial or anticancer agents.
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4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of complex organic molecules. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes. Its benzimidazole moiety also contributes to its use in designing compounds with potential biological activity, such as antimicrobial or anticancer agents.
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