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Catalog Number:
40372
CAS Number:
86-58-8
Quinoline-8-boronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
8-Quinolinylboronic acid, 8-Quinolineboronic acid
Documents
$65.40 /200MG
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Product Information

Quinoline-8-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a quinoline moiety, which enhances its reactivity and makes it an essential building block for the development of various pharmaceuticals and agrochemicals. Its unique structure allows for the formation of stable complexes with diols, making it particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in constructing complex organic molecules. Researchers appreciate its ability to facilitate the synthesis of biologically active compounds, including potential anti-cancer agents and other therapeutic molecules.

In addition to its synthetic applications, Quinoline-8-boronic acid is recognized for its role in the development of sensors and materials due to its ability to selectively bind to certain substrates. This characteristic opens avenues for innovative applications in chemical sensing and environmental monitoring. With its robust performance in various chemical reactions and its potential for creating novel compounds, Quinoline-8-boronic acid stands out as a crucial tool for researchers and industry professionals aiming to advance their projects in organic chemistry and material science.

Synonyms
8-Quinolinylboronic acid, 8-Quinolineboronic acid
CAS Number
86-58-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD01114698
PubChem ID
2734380
Melting Point
> 300 °C
Appearance
White to slightly yellow crystalline powd
Conditions
Store at RT
General Information
Synonyms
8-Quinolinylboronic acid, 8-Quinolineboronic acid
CAS Number
86-58-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD01114698
PubChem ID
2734380
Melting Point
> 300 °C
Appearance
White to slightly yellow crystalline powd
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Quinoline-8-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in medicinal chemistry, particularly in the synthesis of new pharmaceuticals. Its boronic acid functionality allows for the formation of stable complexes with biomolecules, aiding in drug design.
  • Organic Synthesis: It serves as a versatile building block in organic synthesis, enabling the creation of complex organic molecules. Researchers often use it in cross-coupling reactions, which are essential for constructing carbon-carbon bonds.
  • Fluorescent Probes: Quinoline-8-boronic acid can be employed in the development of fluorescent probes for biological imaging. Its ability to bind selectively to certain biomolecules enhances the sensitivity and specificity of imaging techniques.
  • Material Science: In the field of materials science, it is used to modify surfaces and create functional materials. Its unique properties can improve the performance of sensors and catalysts.
  • Environmental Monitoring: This compound can be utilized in the detection of environmental pollutants. Its reactivity with specific contaminants allows for the development of sensitive analytical methods for monitoring water and soil quality.

Citations