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Catalog Number:
17168
CAS Number:
376581-24-7
Quinolin-6-ylboronic acid
Purity:
≥ 95% (HPLC)
Documents
$72.31 /250MG
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Product Information

Quinolin-6-ylboronic acid is a versatile boronic acid derivative known for its significant role in organic synthesis and medicinal chemistry. This compound features a quinoline moiety, which enhances its reactivity and makes it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique properties allow it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules. Researchers and industry professionals utilize Quinolin-6-ylboronic acid for the development of targeted therapies, particularly in oncology, where it can be employed to synthesize compounds that inhibit cancer cell proliferation.

Additionally, Quinolin-6-ylboronic acid exhibits potential in the field of materials science, where it can be used to create functionalized polymers and advanced materials. Its ability to form stable complexes with various substrates makes it a valuable tool in sensor technology and catalysis. With its broad range of applications and effectiveness in enhancing synthetic pathways, Quinolin-6-ylboronic acid stands out as a crucial compound for researchers looking to innovate in both pharmaceutical and material sciences.

CAS Number
376581-24-7
Purity
≥ 95% (HPLC)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD03093100
PubChem ID
4192671
Appearance
Light yellow solid
Conditions
Store at 0 - 8 °C
General Information
CAS Number
376581-24-7
Purity
≥ 95% (HPLC)
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
MDL Number
MFCD03093100
PubChem ID
4192671
Appearance
Light yellow solid
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

Quinolin-6-ylboronic acid is widely utilized in research focused on:

  • Medicinal Chemistry: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in developing anti-cancer agents. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows for the formation of carbon-carbon bonds. This application is vital in creating complex organic molecules for various industries.
  • Material Science: Quinolin-6-ylboronic acid is used in the development of advanced materials, including polymers and nanomaterials. Its unique properties contribute to improved material strength and functionality.
  • Bioconjugation: The compound is utilized in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules. This is particularly beneficial in creating targeted drug delivery systems.
  • Analytical Chemistry: It is applied in the development of sensors and assays for detecting specific biomolecules, enhancing the sensitivity and specificity of analytical methods in clinical diagnostics.

Citations