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499769-95-8

1H-Benzimidazol-4-ylboronic acid

Catalog#: AR003F2B  |   CAS#: 499769-95-8  |   MDL#: MFCD05664677  |   MF: C7H7BN2O2  |   MW: 161.9537

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Catalog Number AR003F2B
Chemical Name 1H-Benzimidazol-4-ylboronic acid
CAS Number 499769-95-8
Molecular Formula C7H7BN2O2
Molecular Weight 161.9537
MDL Number MFCD05664677
SMILES OB(c1cccc2c1nc[nH]2)O

1H-Benzimidazol-4-ylboronic acid is a versatile compound widely utilized in chemical synthesis as a valuable building block in the formation of various organic molecules. Its unique structural properties make it a key component in the creation of pharmaceuticals, agrochemicals, and functional materials.In organic synthesis, 1H-Benzimidazol-4-ylboronic acid serves as a potent precursor for constructing complex molecular structures through Suzuki cross-coupling reactions. This versatile compound readily undergoes cross-coupling with a variety of aryl halides or triflates under mild reaction conditions, enabling efficient and selective formation of carbon-carbon bonds. Additionally, its boronic acid functionality allows for further derivatization through various transformations such as Suzuki-Miyaura, Negishi, or Hiyama coupling reactions, expanding the diversity of compounds that can be accessed.Furthermore, 1H-Benzimidazol-4-ylboronic acid exhibits excellent compatibility with a range of functional groups, making it a valuable tool for the synthesis of bioactive compounds and pharmaceutical intermediates. Its presence in the molecular structure imparts unique physicochemical properties that can enhance the biological activity or material characteristics of the final products.Overall, the application of 1H-Benzimidazol-4-ylboronic acid in chemical synthesis offers researchers and synthetic chemists a powerful tool for the efficient construction of diverse organic molecules with potential applications in drug discovery, materials science, and other fields of research.
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GHS Pictogram N/A
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