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Methyl 6-chloroimidazo[1,2-b]pyridazine-2-carboxylate

  • CAS No. 572910-59-9

  • Cat. No. CS-0042163
  • Purity≥98%
  • MDL No.MFCD11044753

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

Methyl 6-chloroimidazo[1,2-b]pyridazine-2-carboxylate|CS-0042163

Structure of 572910-59-9

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General Information

  • CAS No. 572910-59-9
  • Cat. No. CS-0042163
  • Purity ≥98%
  • MDL No. MFCD11044753
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆ClN₃O₂
  • Molecular Weight 211.61
  • Synonym(s) 6-Chloroimidazo[1,2-b]pyridazine-2-carboxylic acid methyl ester
  • SMILES O=C(C1=CN2N=C(Cl)C=CC2=N1)OC

Description

Methyl 6-chloroimidazo[1,2-b]pyridazine-2-carboxylate is a bench-stable heterocyclic ester featuring a chlorine-substituted imidazopyridazine core. This electron-deficient scaffold integrates readily into synthetic sequences requiring polar, nitrogen-rich intermediates. The methyl ester group enables straightforward derivatization under standard conditions, facilitating access to diverse analogs in medicinal chemistry and materials science applications.

Application

Methyl 6-chloroimidazo[1,2-b]pyridazine-2-carboxylate serves as a versatile building block for the synthesis of imidazopyridazine-based scaffolds. The chloro group at the 6-position enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to medicinally relevant heterocycles in medicinal chemistry and process development 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   56.49
  • LogP   1.1693
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   1

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