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CS-W001157 4
Total: USD 88.00

6-Chloroimidazo[1,2-a]pyrimidine

  • CAS No. 944906-56-3

  • Cat. No. CS-0043967
  • Purity≥98%
  • MDL No.None

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

6-Chloroimidazo[1,2-a]pyrimidine|CS-0043967

Structure of 944906-56-3

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General Information

  • CAS No. 944906-56-3
  • Cat. No. CS-0043967
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₄ClN₃
  • Molecular Weight 153.57
  • Synonym(s) imidazo[1,2-a]pyrimidine,6-chloro
  • SMILES ClC1=CN2C(N=C1)=NC=C2

Description

6-Chloroimidazo[1,2-a]pyrimidine serves as a reactive heterocyclic scaffold for constructing bioactive molecules. This electron-deficient imidazopyrimidine integrates readily into pharmaceutical intermediates and functional materials, offering high stability under standard conditions. The chloro substituent enables direct coupling reactions, streamlining synthetic access to complex architectures in medicinal chemistry and agrochemical development.

Application

6-Chloroimidazo[1,2-a]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of imidazopyrimidine scaffolds prevalent in kinase inhibitors and antiviral agents. The chlorine substituent facilitates palladium-catalyzed cross-coupling reactions, while the fused heterocyclic core exhibits excellent bench stability and compatibility with diverse functional groups. Its predictable reactivity supports straightforward incorporation into complex molecular architectures.

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   30.19
  • LogP   1.3827
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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