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

  • CAS No. 954240-46-1

  • Cat. No. CS-D0156
  • Purity≥95%
  • MDL No.MFCD09701342

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

4-Bromo-6-methylpyridazin-3(2H)-one|CS-D0156

Structure of 954240-46-1

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General Information

  • CAS No. 954240-46-1
  • Cat. No. CS-D0156
  • Purity ≥95%
  • MDL No. MFCD09701342
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₅BrN₂O
  • Molecular Weight 189.01
  • Synonym(s) 5-bromo-3-methyl-1H-pyridazin-6-one
  • SMILES O=C1C(Br)=CC(C)=NN1

Description

4-Bromo-6-methylpyridazin-3(2H)-one features a brominated pyridazinone core with a methyl group at the 6-position, offering a sterically hindered, electron-deficient heterocyclic scaffold. This structure enables direct coupling in late-stage functionalization and serves as a robust building block for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.

Application

4-Bromo-6-methylpyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridazinone scaffolds. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the lactam functionality offers hydrogen-bonding capacity and metabolic stability. The methyl group enhances lipophilicity and provides steric control in downstream transformations. This compound exhibits excellent bench stability, simplifies purification, and functions reliably in standard synthetic workflows for API development.

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   0.84082
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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