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CS-W001157 4
Total: USD 88.00

6-Chloro-3-nitroimidazo[1,2-b]pyridazine

  • CAS No. 18087-76-8

  • Cat. No. CS-W003502
  • Purity≥98%
  • MDL No.MFCD08276991

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

6-Chloro-3-nitroimidazo[1,2-b]pyridazine|CS-W003502

Structure of 18087-76-8

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General Information

  • CAS No. 18087-76-8
  • Cat. No. CS-W003502
  • Purity ≥98%
  • MDL No. MFCD08276991
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₃ClN₄O₂
  • Molecular Weight 198.57
  • Synonym(s) 6-CHLORO-3-NITRO-IMIDAZO[1,2-B]PYRIDAZIN
  • SMILES Clc1ccc2n(n1)c(cn2)[N+](=O)[O-]

Description

6-Chloro-3-nitroimidazo[1,2-b]pyridazine features a fused heterocyclic core bearing a chloro group at the 6-position and a nitro substituent at the 3-position. This electron-deficient scaffold integrates readily into medicinal chemistry campaigns targeting kinase inhibitors and antiparasitic agents, offering enhanced metabolic stability and favorable binding affinity in biological assays.

Application

6-Chloro-3-nitroimidazo[1,2-b]pyridazine serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical synthesis. Its dual functional groups—electrophilic chlorine and electron-deficient nitro moiety—enable selective nucleophilic substitution and coupling reactions under mild conditions. The scaffold exhibits good bench stability and facilitates efficient derivatization, making it well-suited for constructing complex nitrogen-rich frameworks in API development pipelines.

Synthesis

  • Route1

    References

    • ARRAY BIOPHARMA INC.; ANDREWS, Steven, W.; HAAS, Julia; JIANG, Yutong; ZHANG, Gan Patent: WO2010/33941 A1, 2010 ; Location in patent: Page/Page column 35 ; WO 2010/033941 A1

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   73.33
  • LogP   1.2909
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   1

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