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Catalog Number:
26699
CAS Number:
1287753-43-8
[4-Methyl-2-(1H-pyrazol-1-yl)phenyl]boronic acid
Purity:
≥ 95% (NMR)
Documents
$93.14 /250MG
Pack Size Availability Price
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Product Information

[4-Methyl-2-(1H-pyrazol-1-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 participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules. Its unique structure allows for the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its effectiveness in creating diverse compounds, including those with potential applications in cancer treatment and other therapeutic areas.

Additionally, [4-Methyl-2-(1H-pyrazol-1-yl)phenyl]boronic acid exhibits excellent solubility in various organic solvents, enhancing its usability in laboratory settings. Its stability under a range of conditions further supports its application in various synthetic pathways. By incorporating this compound into their research, professionals can streamline their synthesis processes, leading to more efficient development timelines for new drugs and materials.

CAS Number
1287753-43-8
Purity
≥ 95% (NMR)
Molecular Formula
C10H11BN2O2
Molecular Weight
202.0
MDL Number
MFCD08059987
PubChem ID
25248076
Appearance
White to light yellow powder
Conditions
Store at 0-8°C
General Information
CAS Number
1287753-43-8
Purity
≥ 95% (NMR)
Molecular Formula
C10H11BN2O2
Molecular Weight
202.0
MDL Number
MFCD08059987
PubChem ID
25248076
Appearance
White to light yellow 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-Methyl-2-(1H-pyrazol-1-yl)phenyl]boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of pharmaceuticals, particularly in developing targeted therapies for cancer. Its boronic acid functionality allows for the formation of stable complexes with biomolecules, enhancing drug efficacy.
  • Chemical Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for creating complex organic molecules. This application is crucial in the fields of materials science and organic electronics.
  • Biochemical Research: The compound is used in studying enzyme activity and protein interactions due to its ability to form reversible covalent bonds with certain biomolecules, aiding in the understanding of metabolic pathways.
  • Sensor Development: It is utilized in the design of chemical sensors for detecting specific ions or molecules, benefiting environmental monitoring and safety applications by providing sensitive and selective detection methods.
  • Agricultural Chemistry: The compound is being explored for its potential use in developing agrochemicals that can improve crop yields and pest resistance, offering a sustainable approach to modern agriculture.

Citations