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CS-W001157 4
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6-Bromoquinoline-3-carboxylic acid

  • CAS No. 798545-30-9

  • Cat. No. CS-W004890
  • Purity≥95%
  • MDL No.None

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

6-Bromoquinoline-3-carboxylic acid|CS-W004890

Structure of 798545-30-9

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General Information

  • CAS No. 798545-30-9
  • Cat. No. CS-W004890
  • Purity ≥95%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₆BrNO₂
  • Molecular Weight 252.06
  • Synonym(s) 6-bromo-quinoline-3-carboxylic acid
  • SMILES O=C(C1=CC2=CC(Br)=CC=C2N=C1)O

Description

6-Bromoquinoline-3-carboxylic acid features a brominated quinoline core paired with a carboxylic acid group at the 3-position, enabling direct coupling reactions. This electron-deficient heteroaromatic scaffold integrates readily into bioactive molecule frameworks, offering enhanced metabolic stability and predictable reactivity in cross-coupling processes.

Application

6-Bromoquinoline-3-carboxylic acid serves as a versatile building block in medicinal chemistry and materials science, enabling direct functionalization at the quinoline core via Pd-catalyzed cross-coupling reactions. The bromine and carboxylic acid groups provide orthogonal reactivity for late-stage diversification, while the scaffold exhibits excellent bench stability and compatibility with standard purification techniques.

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   50.19
  • LogP   2.6955
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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