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Catalog Number:
17304
CAS Number:
371766-08-4
Ácido isoquinolin-5-borónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Ácido 5-isoquinolinilborónico
Documents
$43.87 /250 mg
Tamaño
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Product Information

Isoquinoline-5-boronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for applications in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds, facilitating the synthesis of complex organic molecules. Researchers have utilized Isoquinoline-5-boronic acid in the preparation of biologically active compounds, including potential anti-cancer agents and other therapeutic molecules, showcasing its relevance in drug discovery and development.

Moreover, Isoquinoline-5-boronic acid's compatibility with various reaction conditions enhances its utility in diverse chemical environments, making it a preferred choice for chemists seeking efficiency and reliability in their synthetic pathways. Its ability to act as a building block in the synthesis of complex heterocycles further underscores its importance in the field of medicinal chemistry. With its proven track record and broad applicability, Isoquinoline-5-boronic acid is an invaluable tool for researchers and industry professionals aiming to innovate and advance their projects.

Synonyms
Ácido 5-isoquinolinilborónico
CAS Number
371766-08-4
Purity
≥ 95 % (HPLC)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD03839356
PubChem ID
599474
Appearance
Gris sólido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 5-isoquinolinilborónico
CAS Number
371766-08-4
Purity
≥ 95 % (HPLC)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD03839356
PubChem ID
599474
Appearance
Gris sólido
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Drug Discovery: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in developing targeted therapies for cancer and other diseases.
  • Bioconjugation: It is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostics.
  • Organic Synthesis: Isoquinoline-5-boronic acid plays a significant role in organic synthesis, particularly in cross-coupling reactions, which are essential for creating complex organic molecules efficiently.
  • Fluorescent Probes: This compound is utilized in creating fluorescent probes for biological imaging, enabling researchers to visualize cellular processes in real-time.
  • Material Science: It finds applications in developing advanced materials, such as polymers and nanomaterials, which can be used in electronics and catalysis.

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