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CS-W001157 4
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6-Bromo-5-methylimidazo[1,2-a]pyrazine

  • CAS No. 1330750-56-5

  • Cat. No. CS-0444708
  • Purity≥97%
  • MDL No.MFCD19982314

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

6-Bromo-5-methylimidazo[1,2-a]pyrazine|CS-0444708

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General Information

  • CAS No. 1330750-56-5
  • Cat. No. CS-0444708
  • Purity ≥97%
  • MDL No. MFCD19982314
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₆BrN₃
  • Molecular Weight 212.05
  • Synonym(s) None
  • SMILES CC1=C(Br)N=CC2=NC=CN12

Description

6-Bromo-5-methylimidazo[1,2-a]pyrazine features a fused heterocyclic core with bromine and methyl substituents at strategic positions, enabling direct functionalization in cross-coupling reactions. The electron-deficient imidazopyrazine scaffold enhances reactivity in transition-metal-catalyzed transformations, while the bench-stable nature supports reliable handling in synthetic workflows.

Application

6-Bromo-5-methylimidazo[1,2-a]pyrazine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the methyl substituent enhances metabolic stability and modulates electronic properties. The fused imidazopyrazine core provides structural rigidity and favorable pharmacophoric characteristics. This compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard synthetic workflows involving C–X bond formation and functional group interconversions.

Safety Information

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GHS Pictogram :
GHS No : GHS06
Signal Word : Danger
UN#: 2811
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H301-H311-H331
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501

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Computational Chemistry Data

  • TPSA   30.19
  • LogP   1.80022
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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