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Catalog Number:
26700
CAS Number:
1287753-42-7
Acide 6-méthyl-5-quinolinyl)boronique
Purity:
≥ 99 % (HPLC)
Documents
$93.14 /250 mg
Taille
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Product Information

(6-Methyl-5-quinolinyl)boronic acid is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of complex organic molecules. Its unique structure, featuring a quinoline moiety, enhances its reactivity and selectivity, which is crucial for developing pharmaceuticals and agrochemicals. Researchers have successfully utilized (6-Methyl-5-quinolinyl)boronic acid in the synthesis of biologically active compounds, showcasing its potential in drug discovery and development.

In addition to its synthetic utility, (6-Methyl-5-quinolinyl)boronic acid exhibits promising properties that make it suitable for various applications in materials science and catalysis. Its ability to form stable complexes with various substrates allows for innovative approaches in designing new materials with tailored functionalities. This compound stands out among similar boronic acids due to its enhanced stability and reactivity, providing researchers and industry professionals with a reliable tool for advancing their projects. Whether in pharmaceutical development or materials innovation, (6-Methyl-5-quinolinyl)boronic acid is a valuable asset for those seeking to push the boundaries of chemical research.

CAS Number
1287753-42-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H10BNO2
Molecular Weight
187.0
MDL Number
MFCD15204354
PubChem ID
51072217
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
CAS Number
1287753-42-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H10BNO2
Molecular Weight
187.0
MDL Number
MFCD15204354
PubChem ID
51072217
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(6-Methyl-5-quinolinyl)boronic acid is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in synthesizing pharmaceutical agents, particularly in targeting specific enzymes and receptors, making it valuable in the development of new medications.
  • Chemical Synthesis: It serves as an important building block in organic synthesis, allowing chemists to create complex molecules efficiently, which is essential in various chemical industries.
  • Bioconjugation: The boronic acid functionality enables the formation of stable bonds with diols, facilitating the development of bioconjugates for drug delivery systems and diagnostic applications.
  • Material Science: This compound is used in the development of advanced materials, particularly in creating sensors and electronic devices due to its unique electronic properties.
  • Research in Catalysis: It is employed in catalytic processes, enhancing reaction rates and selectivity in various chemical reactions, which is beneficial for improving efficiency in industrial applications.

Citations