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3-Aminoquinolin-2(1H)-one

  • CAS No. 5873-00-7

  • Cat. No. CS-0099008
  • Purity≥95%
  • MDL No.MFCD09754189

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

3-Aminoquinolin-2(1H)-one|CS-0099008

Structure of 5873-00-7

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General Information

  • CAS No. 5873-00-7
  • Cat. No. CS-0099008
  • Purity ≥95%
  • MDL No. MFCD09754189
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₈N₂O
  • Molecular Weight 160.17
  • Synonym(s) 3-Aminoquinoline-2(1H)-one
  • SMILES O=C1NC2=C(C=CC=C2)C=C1N

Description

3-Aminoquinolin-2(1H)-one delivers a versatile heterocyclic scaffold with enhanced solubility and stability under standard conditions. This electron-rich moiety integrates readily into medicinal chemistry campaigns, serving as a key building block for kinase inhibitors and fluorescent probes. The amino group enables straightforward derivatization, while the quinolinone core provides robust structural integrity and favorable pharmacokinetic properties.

Application

3-Aminoquinolin-2(1H)-one serves as a versatile scaffold in medicinal chemistry, enabling efficient access to quinoline-based heterocycles through standard functionalization pathways. Its amino and carbonyl groups offer orthogonal reactivity for coupling, derivatization, and metal-catalyzed transformations. The compound exhibits good bench stability and facilitates purification via common techniques, making it well-suited for iterative synthesis and lead optimization campaigns.

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   58.88
  • LogP   1.1103
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   0

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