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CS-W001157 4
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7-Bromo-4-methylquinoline

  • CAS No. 141052-31-5

  • Cat. No. CS-0149200
  • Purity≥95%
  • MDL No.MFCD18204665

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

7-Bromo-4-methylquinoline|CS-0149200

Structure of 141052-31-5

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General Information

  • CAS No. 141052-31-5
  • Cat. No. CS-0149200
  • Purity ≥95%
  • MDL No. MFCD18204665
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₈BrN
  • Molecular Weight 222.08
  • Synonym(s) 4-Methyl-7-broMoquinoline
  • SMILES CC1=CC=NC2=CC(Br)=CC=C12

Description

7-Bromo-4-methylquinoline is a heteroaromatic scaffold featuring a bromine substituent at the 7-position and a methyl group at the 4-position. This combination imparts enhanced electron density and steric profile, facilitating efficient coupling in palladium-catalyzed transformations. The molecule exhibits robust stability under standard reaction conditions and demonstrates favorable solubility in common organic solvents.

Application

7-Bromo-4-methylquinoline serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. The bromo group enables reliable Suzuki, Stille, and Negishi couplings, while the methyl substituent enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by column chromatography, it functions effectively in the synthesis of quinoline-based pharmaceuticals and functional materials.

Synthesis

  • Route1
    • null|null
      78-94-4
    • ~41%
    • In-stock
      7-Bromo-4-methylquinoline|CS-0149200
      141052-31-5

    References

    • ELI LILLY AND COMPANY Patent: WO2004/48383 A1, 2004 ; Location in patent: Page 40-41 ; WO 2004/048383 A1

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   12.89
  • LogP   3.30572
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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