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Catalog Number:
26690
CAS Number:
1226849-25-7
Acide [4-(1 H -pyrazol-5-yl)phényl]boronique
Purity:
≥ 96% (RMN)
Documents
$188.28 /100 mg
Taille
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Product Information

[4-(1H-Pyrazol-5-yl)phenyl]boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to develop pharmaceuticals, agrochemicals, and advanced materials. Its application in the synthesis of biologically active compounds highlights its significance in drug discovery and development, especially in targeting specific pathways in disease mechanisms.

Moreover, [4-(1H-Pyrazol-5-yl)phenyl]boronic acid stands out for its compatibility with various reaction conditions, allowing for greater flexibility in synthetic routes. This compound is also recognized for its potential in sensor technology, particularly in the detection of sugars and other biomolecules, enhancing its relevance in biochemical applications. With its robust performance and broad applicability, this boronic acid is an invaluable asset for researchers aiming to innovate and streamline their synthetic processes.

CAS Number
1226849-25-7
Purity
≥ 96% (RMN)
Molecular Formula
C9H9BN2O2
Molecular Weight
188.0
MDL Number
MFCD06739074
PubChem ID
45791081
Appearance
Poudre beige
Conditions
Conserver à 0-8°C
General Information
CAS Number
1226849-25-7
Purity
≥ 96% (RMN)
Molecular Formula
C9H9BN2O2
Molecular Weight
188.0
MDL Number
MFCD06739074
PubChem ID
45791081
Appearance
Poudre beige
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

[4-(1H-Pyrazol-5-yl)phenyl]boronic acid is widely utilized in research focused on:

  • Drug Development: This compound is instrumental in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies, due to its ability to form stable complexes with biomolecules.
  • Bioconjugation: It serves as a key reagent in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other compounds, enhancing the specificity and efficacy of drug delivery systems.
  • Organic Synthesis: This boronic acid is widely used in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for creating complex organic molecules in materials science and organic chemistry.
  • Sensor Development: It plays a significant role in the fabrication of chemical sensors, particularly for detecting biomolecules, due to its ability to interact selectively with specific targets.
  • Agricultural Chemistry: The compound is also explored for its potential in developing agrochemicals, including herbicides and pesticides, offering a pathway to more effective and environmentally friendly agricultural practices.

Citations