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Catalog Number:
26698
CAS Number:
1025735-46-9
Ácido [3-(3,5-dimetil- 1H- pirazol-1-il)fenil]borónico
Purity:
≥ 99 % (HPLC)
Documents
$127.79 /100 mg
Tamaño
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Product Information

[3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenyl]boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its unique structure, featuring a pyrazole ring, enhances its reactivity and selectivity, making it particularly valuable in the development of pharmaceuticals and agrochemicals. Researchers have successfully employed this compound in the synthesis of various biologically active molecules, showcasing its potential in drug discovery and development.

In addition to its synthetic applications, [3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenyl]boronic acid exhibits promising properties in materials science, particularly in the creation of functionalized polymers and advanced materials. Its ability to act as a building block in the design of novel materials opens avenues for innovation in electronics and nanotechnology. With its robust performance and adaptability, this compound stands out as a key player in both research and industrial applications, offering significant advantages over traditional reagents in terms of efficiency and specificity.

CAS Number
1025735-46-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C11H13BN2O2
Molecular Weight
216.0
MDL Number
MFCD08572151
PubChem ID
16640550
Appearance
Sólido de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1025735-46-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C11H13BN2O2
Molecular Weight
216.0
MDL Number
MFCD08572151
PubChem ID
16640550
Appearance
Sólido de color blanco a blanquecino
Conditions
Conservar entre 0 y 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-(3,5-Dimethyl-1H-pyrazol-1-yl)phenyl]boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing pharmaceuticals, particularly in developing targeted therapies for cancer, enhancing the efficacy of existing drugs.
  • Chemical Sensing: Its unique properties make it suitable for creating sensors that detect specific biomolecules, aiding in diagnostics and environmental monitoring.
  • Organic Electronics: The compound is used in the fabrication of organic semiconductors, contributing to the development of flexible and efficient electronic devices.
  • Material Science: It plays a role in creating advanced materials with tailored properties, such as improved thermal stability and mechanical strength, which are essential in various industrial applications.
  • Research in Catalysis: This boronic acid derivative is utilized in catalytic processes, facilitating reactions that are crucial in organic synthesis, thus improving reaction efficiency and selectivity.

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