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CS-W001157 4
Total: USD 88.00

6-Bromo-7-methylquinoline

  • CAS No. 122759-89-1

  • Cat. No. CS-W007221
  • Purity≥98%
  • MDL No.MFCD18260428

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

6-Bromo-7-methylquinoline|CS-W007221

Structure of 122759-89-1

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General Information

  • CAS No. 122759-89-1
  • Cat. No. CS-W007221
  • Purity ≥98%
  • MDL No. MFCD18260428
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₈BrN
  • Molecular Weight 222.08
  • Synonym(s) None
  • SMILES CC1=C(Br)C=C2C=CC=NC2=C1

Description

6-Bromo-7-methylquinoline is a heterocyclic scaffold featuring bromine at the 6-position and a methyl group at the 7-position, enabling selective functionalization in cross-coupling reactions. This electron-deficient quinoline derivative exhibits enhanced solubility and stability under standard conditions, facilitating its use in medicinal chemistry and materials synthesis.

Application

6-Bromo-7-methylquinoline serves as a versatile building block in medicinal chemistry and catalytic synthesis, enabling direct functionalization at the C6 position via palladium-catalyzed cross-coupling. The methyl group at C7 enhances electron density, improving reactivity in electrophilic substitution and facilitating downstream derivatization. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing complex heterocyclic scaffolds in API development.

Synthesis

  • Route1

    References

    • SGX PHARMACEUTICALS, INC. Patent: WO2008/51808 A2, 2008 ; Location in patent: Page/Page column 79-80 ; WO 2008/051808 A2

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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