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CS-W001157 4
Total: USD 88.00

6-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde

  • CAS No. 30384-96-4

  • Cat. No. CS-W022471
  • Purity≥98%
  • MDL No.MFCD09864909

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

6-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde|CS-W022471

Structure of 30384-96-4

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General Information

  • CAS No. 30384-96-4
  • Cat. No. CS-W022471
  • Purity ≥98%
  • MDL No. MFCD09864909
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₅BrN₂O
  • Molecular Weight 225.04
  • Synonym(s) 6-BROMOIMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE
  • SMILES BrC2=C[N]1C(=NC=C1C=O)C=C2

Description

6-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde features a brominated imidazopyridine core paired with a reactive aldehyde group, enabling direct functionalization in cross-coupling and conjugation workflows. The electron-deficient heterocycle enhances compatibility with nucleophilic attack, while the aldehyde facilitates rapid derivatization under mild conditions. This scaffold delivers high stability and predictable reactivity in synthetic medicinal chemistry and materials development.

Application

6-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of pharmacologically relevant scaffolds. Its bromo and aldehyde functionalities provide orthogonal handles for Pd-catalyzed cross-coupling and condensation reactions, facilitating rapid diversification in medicinal chemistry campaigns. The compound exhibits good bench stability and is amenable to standard purification techniques, making it well-suited for high-throughput synthetic workflows.

Safety Information

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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   34.37
  • LogP   1.9093
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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