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CS-W001157 4
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3-Bromo-7-iodoquinoline

  • CAS No. 1354223-46-3

  • Cat. No. CS-0062122
  • Purity≥97%
  • MDL No.MFCD28679234

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

3-Bromo-7-iodoquinoline|CS-0062122

Structure of 1354223-46-3

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General Information

  • CAS No. 1354223-46-3
  • Cat. No. CS-0062122
  • Purity ≥97%
  • MDL No. MFCD28679234
  • Storage RT, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₅BrIN
  • Molecular Weight 333.95
  • Synonym(s) None
  • SMILES N1=CC(=CC2=CC=C(C=C12)I)Br

Description

3-Bromo-7-iodoquinoline features a quinoline core with halogens at electron-deficient positions, enabling selective cross-coupling reactions. The bromine and iodine substituents facilitate palladium-catalyzed transformations, while the planar aromatic system enhances π-stacking interactions in materials applications. This derivative offers high reactivity and stability under standard conditions.

Application

3-Bromo-7-iodoquinoline serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling sequential functionalization at both halogen sites. The bromine and iodine substituents exhibit complementary reactivity, facilitating orthogonal coupling strategies in the synthesis of complex quinoline-based scaffolds. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for medicinal chemistry and process development workflows.

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   3.6019
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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