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

  • CAS No. 892874-34-9

  • Cat. No. CS-0041433
  • Purity≥97%
  • MDL No.MFCD08437554

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

7-Bromoquinoline-3-carboxylic acid|CS-0041433

Structure of 892874-34-9

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General Information

  • CAS No. 892874-34-9
  • Cat. No. CS-0041433
  • Purity ≥97%
  • MDL No. MFCD08437554
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₆BrNO₂
  • Molecular Weight 252.06
  • Synonym(s) 7-Bromo-3-quinolinecarboxylic acid
  • SMILES OC(=O)C1=CC2=C(C=C(Br)C=C2)N=C1

Description

7-Bromoquinoline-3-carboxylic acid features a bromine substituent at the 7-position and a carboxylic acid group at the 3-position of the quinoline scaffold. This electron-deficient heterocycle integrates readily into synthetic routes requiring halogenation or coupling reactions. The polar carboxylic acid moiety enhances solubility in polar solvents and facilitates derivatization. Its bench-stable, moisture-tolerant structure supports reliable handling under standard laboratory conditions.

Application

7-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 bromo group facilitates efficient Suzuki, Stille, or Negishi transformations, while the carboxylic acid provides a handle for amide coupling, esterification, or metal complexation. Its stability under standard synthetic conditions and compatibility with diverse reaction environments make it a practical choice for constructing bioactive heterocycles and conjugated systems.

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-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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