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CS-W001157 4
Total: USD 88.00

3-Bromo-7-methylimidazo[1,2-a]pyridine

  • CAS No. 56051-32-2

  • Cat. No. CS-0038367
  • Purity≥96%
  • MDL No.None

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

3-Bromo-7-methylimidazo[1,2-a]pyridine|CS-0038367

Structure of 56051-32-2

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General Information

  • CAS No. 56051-32-2
  • Cat. No. CS-0038367
  • Purity ≥96%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇BrN₂
  • Molecular Weight 211.06
  • Synonym(s) 3-BROMO-7-METHYL-IMIDAZO[1,2-A]PYRIDINE
  • SMILES CC1=CC2=NC=C(Br)N2C=C1

Description

3-Bromo-7-methylimidazo[1,2-a]pyridine is a heteroaromatic building block featuring a bromine substituent at the 3-position and a methyl group at the 7-position. This configuration enables selective functionalization in transition-metal-catalyzed coupling reactions. The compound exhibits enhanced solubility in organic solvents and stability under standard bench conditions, facilitating its integration into complex synthetic sequences for pharmaceutical and agrochemical discovery.

Application

3-Bromo-7-methylimidazo[1,2-a]pyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biologically relevant heterocyclic scaffolds. The bromo group facilitates efficient C–C and C–N bond formation under standard conditions, while the imidazopyridine core provides structural rigidity and favorable pharmacophoric properties. Bench-stable and compatible with diverse functional groups, it functions effectively in modular synthesis workflows for kinase inhibitors and other targeted therapeutics.

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   17.3
  • LogP   2.40522
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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