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CS-W001157 4
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Imidazo[1,2-a]pyridine-6-boronic acid

  • CAS No. 913835-63-9

  • Cat. No. CS-0046237
  • Purity≥97%
  • MDL No.MFCD06739225

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

Imidazo[1,2-a]pyridine-6-boronic acid|CS-0046237

Structure of 913835-63-9

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General Information

  • CAS No. 913835-63-9
  • Cat. No. CS-0046237
  • Purity ≥97%
  • MDL No. MFCD06739225
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₇BN₂O₂
  • Molecular Weight 161.95
  • Synonym(s) 9-Azoindole-5-boric acid
  • SMILES OB(C1=CN2C(C=C1)=NC=C2)O

Description

Imidazo[1,2-a]pyridine-6-boronic acid features a rigid heteroaromatic core with a boronic acid handle at the 6-position, enabling direct functionalization in Suzuki-Miyaura coupling. This bench-stable reagent integrates readily into complex molecular architectures, particularly in medicinal chemistry and materials science applications requiring fused nitrogen-containing scaffolds.

Application

Imidazo[1,2-a]pyridine-6-boronic acid serves as a versatile building block for 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 scaffolds. Its incorporation into heterocyclic frameworks supports the synthesis of advanced medicinal chemistry intermediates and target-oriented libraries.

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   57.76
  • LogP   -0.9859
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   1

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