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Catalog Number:
17026
CAS Number:
355386-94-6
Quinoline-5-boronic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
5-Quinolineboronic acid
Documents
$110.57 /250MG
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Product Information

Quinoline-5-boronic acid is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative features a quinoline moiety, which enhances its reactivity and selectivity in various chemical reactions. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex organic molecules. Researchers and industry professionals utilize Quinoline-5-boronic acid in the development of pharmaceuticals, agrochemicals, and advanced materials, making it a critical building block in synthetic chemistry.

In addition to its role in cross-coupling reactions, Quinoline-5-boronic acid exhibits potential as a ligand in coordination chemistry, contributing to the design of novel catalysts. Its unique properties allow for the modification of existing compounds, leading to the discovery of new therapeutic agents. With its ability to facilitate diverse synthetic pathways, Quinoline-5-boronic acid stands out as an essential tool for chemists aiming to innovate and streamline their research and development processes.

Synonyms
5-Quinolineboronic acid
CAS Number
355386-94-6
Purity
≥ 95% (HPLC)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD03095058
PubChem ID
5153389
Appearance
Light yellow to brown powder
Conditions
Store at 0-8 °C
General Information
Synonyms
5-Quinolineboronic acid
CAS Number
355386-94-6
Purity
≥ 95% (HPLC)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD03095058
PubChem ID
5153389
Appearance
Light yellow to brown powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Quinoline-5-boronic acid is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a crucial building block in the development of various pharmaceutical agents, particularly in creating compounds with anti-cancer properties.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Organic Electronics: Quinoline-5-boronic acid is used in the fabrication of organic semiconductors, contributing to the development of flexible electronic devices and displays.
  • Chemical Sensors: This compound is applied in the design of chemical sensors, providing sensitive detection of environmental pollutants or biological markers.
  • Cross-Coupling Reactions: It plays a significant role in cross-coupling reactions, a vital process in organic synthesis that allows for the formation of carbon-carbon bonds, facilitating the creation of complex organic molecules.

Citations