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Catalog Number:
28478
CAS Number:
128676-84-6
Ácido 2-cloroquinolina-3-borónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Ácido (2-cloro-3-quinolinil)borónico
Documents
$51.18 /1G
Tamaño
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Información del producto

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.

Número CAS
128676-84-6
Fórmula molecular
C9H7BClNO2
Peso molecular
207.42
Número MDL
MFCD01114675
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
128676-84-6
Fórmula molecular
C9H7BClNO2
Peso molecular
207.42
Número MDL
MFCD01114675
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

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.

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