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CS-W001157 4
Total: USD 88.00

(1h-Benzo[d]imidazol-6-yl)boronic acid

  • CAS No. 1228183-22-9

  • Cat. No. CS-0175278
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

(1h-Benzo[d]imidazol-6-yl)boronic acid|CS-0175278

Structure of 1228183-22-9

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General Information

  • CAS No. 1228183-22-9
  • Cat. No. CS-0175278
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₇BN₂O₂
  • Molecular Weight 161.95
  • Synonym(s) (1H-Benzo[d]imidazol-5-yl)boronic acid
  • SMILES OB(O)C1=CC(NC=N2)=C2C=C1

Description

This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, offering robust stability and compatibility with diverse functional groups. The benzimidazole scaffold enhances solubility and electronic modulation, enabling efficient C–C bond formation under standard conditions.

Application

(1H-Benzo[d]imidazol-6-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures under mild conditions. The boronic acid moiety exhibits excellent bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular frameworks. Its incorporation into heterocyclic scaffolds supports the synthesis of pharmaceutically relevant compounds and advanced materials.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   69.14
  • LogP   -0.7573
  • H_Acceptors   3
  • H_Donors   3
  • Rotatable_Bonds   1

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