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CS-W001157 4
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6-Chloro-5-methylpyridazin-3(2H)-one

  • CAS No. 1703-07-7

  • Cat. No. CS-W019006
  • Purity≥95%
  • MDL No.None

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

6-Chloro-5-methylpyridazin-3(2H)-one|CS-W019006

Structure of 1703-07-7

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General Information

  • CAS No. 1703-07-7
  • Cat. No. CS-W019006
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₅ClN₂O
  • Molecular Weight 144.56
  • Synonym(s) 6-chloro-5-methyl-2H-pyridazin-3-one
  • SMILES O=C1C=C(C)C(Cl)=NN1

Description

6-Chloro-5-methylpyridazin-3(2H)-one features a fused heterocyclic core with orthogonal electron-withdrawing and electron-donating substituents, enabling selective reactivity in transition-metal-catalyzed couplings. The chloro group serves as a robust handle for cross-coupling transformations, while the methyl moiety enhances solubility and modulates electronic properties. This scaffold demonstrates stability under standard bench conditions and integrates efficiently into complex molecular architectures.

Application

6-Chloro-5-methylpyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridazinones via palladium-catalyzed cross-coupling reactions. The chloro group facilitates nucleophilic substitution under mild conditions, while the methyl and lactam functionalities provide orthogonal reactivity for downstream derivatization. This compound exhibits excellent bench stability and is compatible with common purification methods, making it well-suited for high-throughput synthesis of bioactive heterocycles.

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   45.75
  • LogP   0.73172
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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