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Catalog Number:
18041
CAS Number:
476620-22-1
3-Pyrazol-1-yl-phenylboronic acid
Purity:
≥ 95% (NMR)
Synonym(s):
[3-(1H-pyrazol-1-yl)phenyl]boronic acid
Documents
$55.48 /100MG
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Product Information

3-Pyrazol-1-yl-phenylboronic acid is a versatile compound that plays a significant role in various fields, particularly in medicinal chemistry and organic synthesis. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of pharmaceuticals and agrochemicals. Its unique pyrazole moiety enhances its reactivity and selectivity, allowing researchers to utilize it in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the synthesis of complex organic molecules.

In addition to its applications in synthetic chemistry, 3-Pyrazol-1-yl-phenylboronic acid has shown potential in the development of targeted therapies, particularly in oncology, where it can be used to create compounds that selectively inhibit tumor growth. Its compatibility with various functional groups and ease of modification make it a valuable tool for researchers aiming to innovate in drug design and development. The compound's stability and efficiency in reactions further underscore its importance in both academic and industrial settings, making it a preferred choice for professionals seeking reliable and effective reagents.

Synonyms
[3-(1H-pyrazol-1-yl)phenyl]boronic acid
CAS Number
476620-22-1
Purity
≥ 95% (NMR)
Molecular Formula
C9H9BN2O2
Molecular Weight
187.99
MDL Number
MFCD05864582
PubChem ID
16640530
Appearance
Light yellow to off white powder
Conditions
Store at 0-8°C
General Information
Synonyms
[3-(1H-pyrazol-1-yl)phenyl]boronic acid
CAS Number
476620-22-1
Purity
≥ 95% (NMR)
Molecular Formula
C9H9BN2O2
Molecular Weight
187.99
MDL Number
MFCD05864582
PubChem ID
16640530
Appearance
Light yellow to off white powder
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

3-Pyrazol-1-yl-phenylboronic acid is widely utilized in research focused on:

  • Medicinal Chemistry: This compound plays a crucial role in the development of new pharmaceuticals, particularly in targeting specific enzymes and receptors, enhancing drug efficacy.
  • Organic Synthesis: It serves as a versatile building block in the synthesis of complex organic molecules, allowing chemists to create diverse compounds efficiently.
  • Bioconjugation: The ability to form stable bonds with biomolecules makes it valuable in creating targeted drug delivery systems, improving therapeutic outcomes.
  • Material Science: Utilized in the development of advanced materials, it contributes to the creation of sensors and catalysts with enhanced performance characteristics.
  • Agricultural Chemistry: This compound is explored for its potential use in developing agrochemicals that can improve crop yield and resistance to pests, addressing food security challenges.

Citations