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Catalog Number:
30418
CAS Number:
5720-05-8
Acide p -tolylboronique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide 4-méthylphénylboronique
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Product Information

<p>p-Tolylboronic acid is a versatile organoboron compound widely recognized for its utility in organic synthesis and medicinal chemistry. This compound, characterized by its ability to form stable complexes with various substrates, is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds. Researchers and industry professionals utilize p-Tolylboronic acid to synthesize complex organic molecules, including pharmaceuticals and agrochemicals, enhancing the efficiency and selectivity of their reactions. Its favorable properties, such as high solubility in organic solvents and compatibility with a range of functional groups, make it an ideal choice for diverse applications in both academic and industrial settings.</p>

<p>Moreover, p-Tolylboronic acid serves as a crucial building block in the development of biologically active compounds, contributing to advancements in drug discovery and development. Its unique ability to participate in various coupling reactions allows for the rapid assembly of complex structures, streamlining the synthesis process. With its proven track record in enhancing reaction yields and simplifying synthetic pathways, p-Tolylboronic acid stands out as a key reagent for chemists aiming to innovate and optimize their research.</p>

Synonyms
Acide 4-méthylphénylboronique
CAS Number
5720-05-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C7H9BO2
Molecular Weight
135.96
MDL Number
MFCD00039138
PubChem ID
79799
Melting Point
256-263 ?C
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide 4-méthylphénylboronique
CAS Number
5720-05-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C7H9BO2
Molecular Weight
135.96
MDL Number
MFCD00039138
PubChem ID
79799
Melting Point
256-263 ?C
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

p-Tolylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of various organic molecules, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions, which are essential in creating complex pharmaceuticals and agrochemicals.
  • Pharmaceutical Development: Its ability to form stable complexes with certain biomolecules makes it valuable in drug design, allowing researchers to develop targeted therapies with improved efficacy and reduced side effects.
  • Material Science: p-Tolylboronic acid is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and strength, which are vital in electronics and coatings.
  • Biochemistry: In biochemical research, it acts as a reagent for the selective labeling of glycoproteins and other biomolecules, facilitating the study of cellular processes and disease mechanisms.
  • Environmental Chemistry: The compound is also explored for its potential in environmental applications, such as the removal of pollutants from water, showcasing its versatility and importance in sustainability efforts.

Citations