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CS-W001157 4
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2-Bromoimidazo[2,1-b]thiazole

  • CAS No. 944581-09-3

  • Cat. No. CS-M1244
  • Purity≥98%
  • MDL No.MFCD11036022

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

2-Bromoimidazo[2,1-b]thiazole|CS-M1244

Structure of 944581-09-3

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General Information

  • CAS No. 944581-09-3
  • Cat. No. CS-M1244
  • Purity ≥98%
  • MDL No. MFCD11036022
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₃BrN₂S
  • Molecular Weight 203.06
  • Synonym(s) 2-Bromo-imidazo[2,1-b]thiazole
  • SMILES BrC1=CN2C(S1)=NC=C2

Description

2-Bromoimidazo[2,1-b]thiazole delivers a reactive halogen site for cross-coupling and functionalization in heterocyclic synthesis. The fused imidazo[2,1-b]thiazole core provides enhanced stability and electron-deficient character, enabling efficient integration into complex molecular architectures under standard conditions.

Application

2-Bromoimidazo[2,1-b]thiazole serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the imidazo[2,1-b]thiazole core provides robust stability and favorable electronic properties. Its functional group tolerance facilitates integration into complex molecular architectures, making it a reliable scaffold for drug discovery and materials science applications.

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   17.3
  • LogP   2.1583
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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