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CS-W001157 4
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7-Bromo-2-quinolinecarboxylic acid

  • CAS No. 1057217-63-6

  • Cat. No. CS-W008858
  • Molecule weight252.06
  • Purity≥97%
  • MDL No.MFCD11108693

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

7-Bromo-2-quinolinecarboxylic acid|CS-W008858

Structure of 1057217-63-6

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General Information

  • CAS No. 1057217-63-6
  • Cat. No. CS-W008858
  • Purity ≥97%
  • MDL No. MFCD11108693
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₆BrNO₂
  • Molecular Weight 252.06
  • Synonym(s) 7-Bromoquinoline-2-carboxylic acid
  • SMILES O=C(C1=NC2=CC(Br)=CC=C2C=C1)O

Description

7-Bromo-2-quinolinecarboxylic acid features a bromine substituent at the 7-position of the quinoline scaffold, enhancing electrophilic reactivity and enabling direct functionalization in cross-coupling reactions. The carboxylic acid group provides a handle for derivatization, while the planar heteroaromatic core imparts stability and favorable solubility in polar organic solvents. This compound serves as a key intermediate in medicinal chemistry and materials synthesis.

Application

7-Bromo-2-quinolinecarboxylic acid serves as a versatile building block for medicinal chemistry and materials science, enabling direct incorporation into biologically active heterocycles via standard coupling reactions. Its bromine and carboxylic acid functionalities provide orthogonal reactivity for palladium-catalyzed cross-couplings and amide bond formation, with excellent bench stability and straightforward purification.

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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