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CS-W001157 4
Total: USD 88.00

4-Bromo-1-methylquinolin-2(1H)-one

  • CAS No. 941-72-0

  • Cat. No. CS-0151125
  • Purity≥97%
  • MDL No.MFCD11858574

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

4-Bromo-1-methylquinolin-2(1H)-one|CS-0151125

Structure of 941-72-0

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General Information

  • CAS No. 941-72-0
  • Cat. No. CS-0151125
  • Purity ≥97%
  • MDL No. MFCD11858574
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₈BrNO
  • Molecular Weight 238.08
  • Synonym(s) 4-bromo-1-methylquinolin-2-one
  • SMILES CN1C2=CC=CC=C2C(=CC1=O)Br

Description

4-Bromo-1-methylquinolin-2(1H)-one features a brominated quinolinone scaffold with enhanced electronic modulation from the methyl group at C1. This bench-stable, moisture-tolerant heterocycle integrates readily into transition-metal-catalyzed coupling reactions and serves as a key intermediate in medicinal chemistry for constructing complex nitrogen-containing frameworks.

Application

4-Bromo-1-methylquinolin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent. The quinolinone core provides a rigid, planar scaffold with hydrogen-bonding capacity, facilitating interactions in target binding. Its methyl group enhances lipophilicity and metabolic stability, while the keto-enol tautomerism supports diverse derivatization pathways. Bench-stable and readily purified by crystallization, it functions effectively in modular synthesis of kinase inhibitors and other 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   22
  • LogP   2.301
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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