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Catalog Number:
17322
CAS Number:
376584-63-3
1H-Pyrazol-3-yl boronic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
3-Pyrazole-boronic acid
Documents
$55.48 /1G
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Product Information

1H-Pyrazol-3-yl 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. Researchers and industry professionals leverage its unique properties to synthesize a variety of biologically active compounds, including pharmaceuticals and agrochemicals. Its application in the development of targeted therapies showcases its potential in advancing drug discovery, particularly in the fields of oncology and infectious diseases.

Additionally, 1H-Pyrazol-3-yl boronic acid is valued for its role in the preparation of functionalized materials and sensors, enhancing its relevance in materials science. The compound's stability and reactivity under mild conditions make it an attractive choice for researchers seeking efficient synthetic pathways. With its growing importance in various sectors, this compound stands out as a key player in innovative research and development, offering significant advantages over traditional reagents in terms of selectivity and yield.

Synonyms
3-Pyrazole-boronic acid
CAS Number
376584-63-3
Purity
≥ 95% (HPLC)
Molecular Formula
C3H5BN2O2
Molecular Weight
111.9
MDL Number
MFCD02020768
PubChem ID
11251979
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
3-Pyrazole-boronic acid
CAS Number
376584-63-3
Purity
≥ 95% (HPLC)
Molecular Formula
C3H5BN2O2
Molecular Weight
111.9
MDL Number
MFCD02020768
PubChem ID
11251979
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

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

  • Drug Development: This compound serves as an important building block in the synthesis of pharmaceuticals, particularly in developing new anti-cancer agents.
  • Organic Synthesis: It is used in various organic reactions, including Suzuki coupling, which is essential for creating complex organic molecules in materials science.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it useful in creating targeted drug delivery systems and biomaterials.
  • Sensor Technology: Its ability to interact with specific biomolecules makes it valuable in developing sensors for detecting glucose and other analytes in medical diagnostics.
  • Agricultural Chemistry: It is explored for use in developing agrochemicals, enhancing crop protection products through its reactivity and selectivity.

Citations