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Catalog Number:
26706
CAS Number:
1287753-34-7
[4-Methoxy-2-(1H-pyrazol-1-yl)phenyl]boronic acid
Purity:
≥ 95% (NMR)
Documents
$99.85 /100MG
Pack Size Availability Price
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Product Information

[4-Methoxy-2-(1H-pyrazol-1-yl)phenyl]boronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a methoxy group and a pyrazole moiety, enhances its reactivity and selectivity in various chemical transformations. Researchers and industry professionals can leverage this compound in the development of novel materials and biologically active compounds, particularly in the fields of drug discovery and development.

In addition to its synthetic utility, [4-Methoxy-2-(1H-pyrazol-1-yl)phenyl]boronic acid exhibits potential applications in the development of sensors and catalysts. Its ability to form stable complexes with various substrates allows for the exploration of innovative applications in catalysis and environmental monitoring. The compound's favorable properties, such as solubility and stability, make it an attractive choice for researchers looking to enhance their synthetic methodologies or develop new applications in materials science.

CAS Number
1287753-34-7
Purity
≥ 95% (NMR)
Molecular Formula
C10H11BN2O3
Molecular Weight
218.0
MDL Number
MFCD08059988
PubChem ID
45791109
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
1287753-34-7
Purity
≥ 95% (NMR)
Molecular Formula
C10H11BN2O3
Molecular Weight
218.0
MDL Number
MFCD08059988
PubChem ID
45791109
Appearance
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

[4-Methoxy-2-(1H-pyrazol-1-yl)phenyl]boronic acid is widely utilized in research focused on:

  • Medicinal Chemistry: This compound plays a crucial role in the development of new pharmaceuticals, particularly in the synthesis of targeted therapies for cancer treatment, enhancing drug efficacy.
  • Organic Synthesis: It serves as a versatile building block in organic synthesis, allowing researchers to create complex molecules efficiently through Suzuki coupling reactions.
  • Bioconjugation: The boronic acid functional group enables selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules in diagnostic applications.
  • Material Science: This compound is explored in the development of advanced materials, including polymers and nanomaterials, due to its unique chemical properties that enhance material performance.
  • Analytical Chemistry: It is employed in various analytical methods, including chromatography, to improve the detection and quantification of specific analytes in complex mixtures.

Citations