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Catalog Number:
28478
CAS Number:
128676-84-6
2-Chloroquinoline-3-boronic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
(2-Chloro-3-quinolinyl)boronic acid
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Product Information

2-Chloroquinoline-3-boronic acid is a versatile compound widely utilized in pharmaceutical and chemical research. This boronic acid derivative is particularly valuable in the synthesis of complex organic molecules, serving as a key building block in the development of various medicinal compounds. Its unique structure allows for effective participation in Suzuki coupling reactions, making it an essential reagent for creating biaryl compounds that are crucial in drug discovery and development.

In addition to its applications in organic synthesis, 2-Chloroquinoline-3-boronic acid has shown promise in the field of materials science, where it can be employed in the development of advanced materials with tailored properties. Researchers appreciate its stability and reactivity, which facilitate the formation of diverse chemical architectures. This compound stands out for its ability to enhance the efficiency of synthetic pathways, thereby reducing the time and resources needed for research and development projects.

Synonyms
(2-Chloro-3-quinolinyl)boronic acid
CAS Number
128676-84-6
Purity
≥ 95% (HPLC)
Molecular Formula
C9H7BClNO2
Molecular Weight
207.42
MDL Number
MFCD01114675
PubChem ID
4198643
Appearance
Off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
(2-Chloro-3-quinolinyl)boronic acid
CAS Number
128676-84-6
Purity
≥ 95% (HPLC)
Molecular Formula
C9H7BClNO2
Molecular Weight
207.42
MDL Number
MFCD01114675
PubChem ID
4198643
Appearance
Off-white 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

2-Chloroquinoline-3-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key building block in the synthesis of various pharmaceutical agents, particularly those targeting cancer and infectious diseases.
  • Organic Synthesis: It is employed in cross-coupling reactions, which are essential for creating complex organic molecules, making it valuable in the development of new materials and chemicals.
  • Bioconjugation: The unique properties of this boronic acid facilitate the attachment of biomolecules, enhancing drug delivery systems and improving the efficacy of therapeutic agents.
  • Fluorescent Probes: Researchers utilize this compound in the creation of fluorescent probes for biological imaging, allowing for real-time tracking of cellular processes.
  • Environmental Applications: It is also being explored for use in the detection and removal of pollutants, showcasing its potential in environmental chemistry and sustainability efforts.

Citations