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CS-W001157 4
Total: USD 88.00

6-Bromo-3-iodoquinolin-4-ol

  • CAS No. 1260886-58-5

  • Cat. No. CS-0334678
  • Molecule weight349.95
  • Purity≥96%
  • MDL No.None

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

6-Bromo-3-iodoquinolin-4-ol|CS-0334678

Structure of 1260886-58-5

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General Information

  • CAS No. 1260886-58-5
  • Cat. No. CS-0334678
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₅BrINO
  • Molecular Weight 349.95
  • Synonym(s) None
  • SMILES OC1=C(I)C=NC2=CC=C(Br)C=C12

Description

6-Bromo-3-iodoquinolin-4-ol features a quinolin-4-ol scaffold bearing bromo and iodo substituents at the 6- and 3-positions, respectively. This electron-deficient heterocycle integrates readily into cross-coupling workflows, enabling efficient access to complex polycyclic architectures. The hydroxyl group enhances solubility and provides a handle for derivatization.

Application

6-Bromo-3-iodoquinolin-4-ol serves as a versatile building block for the synthesis of functionalized quinoline scaffolds. The molecule features orthogonal halogen handles—bromine at C6 and iodine at C3—that enable sequential cross-coupling reactions under palladium catalysis. Its phenolic OH group provides a site for derivatization or metal coordination, enhancing utility in medicinal chemistry and materials science applications. Bench-stable and compatible with standard purification methods, it facilitates efficient access to complex heterocyclic architectures.

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-P330-P362-P405-P501

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Computational Chemistry Data

  • TPSA   33.12
  • LogP   3.3075
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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