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Catalog Number:
40373
CAS Number:
191162-39-7
Quinoline-3-boronic acid
Purity:
≥ 95% (Assay by tiration)
Synonym(s):
3-Quinolineboronic acid, (3-Quinolinyl)boronic acid, Quinolin-3-ylboronic acid
Documents
$84.83 /1G
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Product Information

Quinoline-3-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential reagent for the formation of carbon-carbon bonds. Its unique structure allows for the introduction of quinoline moieties into various organic frameworks, which is particularly valuable in the development of pharmaceuticals and agrochemicals. Researchers appreciate its role in synthesizing complex molecules, including biologically active compounds that exhibit anti-cancer and anti-inflammatory properties.

In addition to its synthetic applications, Quinoline-3-boronic acid serves as a key building block in the preparation of fluorescent probes and sensors. Its compatibility with diverse functional groups enhances its utility in various chemical transformations, making it a preferred choice for chemists seeking efficiency and reliability in their reactions. With its proven track record in facilitating innovative research and development, Quinoline-3-boronic acid stands out as a crucial tool for professionals in the fields of chemistry and materials science.

Synonyms
3-Quinolineboronic acid, (3-Quinolinyl)boronic acid, Quinolin-3-ylboronic acid
CAS Number
191162-39-7
Purity
≥ 95% (Assay by tiration)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD02183527
PubChem ID
2734663
Melting Point
191 - 196 °C
Appearance
White to light yellow to dark green cryst
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Quinolineboronic acid, (3-Quinolinyl)boronic acid, Quinolin-3-ylboronic acid
CAS Number
191162-39-7
Purity
≥ 95% (Assay by tiration)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD02183527
PubChem ID
2734663
Melting Point
191 - 196 °C
Appearance
White to light yellow to dark green cryst
Conditions
Store at 2 - 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-3-boronic acid is widely utilized in research focused on:

  • Drug Discovery: It serves as a key building block in the synthesis of pharmaceutical compounds, particularly in the development of new anti-cancer agents.
  • Chemical Synthesis: This compound is used in various organic reactions, including Suzuki coupling, which is essential for creating complex organic molecules.
  • Material Science: It plays a role in the development of advanced materials, such as polymers and nanomaterials, enhancing their properties for specific applications.
  • Biochemistry: Quinoline-3-boronic acid is utilized in the study of enzyme inhibitors, helping researchers understand biochemical pathways and develop targeted therapies.
  • Analytical Chemistry: It is employed in the detection and quantification of specific biomolecules, providing valuable insights in clinical and environmental analysis.

Citations