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Catalog Number:
40139
CAS Number:
63139-21-9
Acide 4-éthylphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-éthylbenzèneboronique
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Product Information

4-Ethylphenylboronic acid is a versatile organoboron compound that plays a crucial role in various chemical applications, particularly in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique properties allow for the efficient synthesis of biaryl compounds, which are significant in the development of pharmaceuticals and agrochemicals. Researchers appreciate its effectiveness in enhancing the selectivity and yield of reactions, thereby streamlining the synthesis process.

In addition to its applications in organic synthesis, 4-Ethylphenylboronic acid is also utilized in the development of sensors and materials due to its boron functionality. Its ability to interact with various substrates makes it a valuable component in the design of advanced materials and drug delivery systems. The compound's stability and reactivity provide significant advantages over similar boronic acids, making it a preferred choice for professionals seeking reliable and efficient solutions in their research and industrial applications.

Synonyms
Acide 4-éthylbenzèneboronique
CAS Number
63139-21-9
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 2
Molecular Weight
149.98
MDL Number
MFCD00859377
PubChem ID
2734352
Melting Point
141 °C (lit.)
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-éthylbenzèneboronique
CAS Number
63139-21-9
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 2
Molecular Weight
149.98
MDL Number
MFCD00859377
PubChem ID
2734352
Melting Point
141 °C (lit.)
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Ethylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently. Its ability to form stable complexes with various substrates makes it invaluable in developing pharmaceuticals and agrochemicals.
  • Bioconjugation: Researchers leverage its boronic acid functionality to attach biomolecules, such as proteins and nucleic acids, to surfaces or other molecules. This application is crucial in developing biosensors and drug delivery systems.
  • Diagnostics: The compound is used in the design of diagnostic tools, particularly in detecting glucose levels in blood. Its interaction with diols allows for the development of sensitive and selective glucose sensors, benefiting diabetes management.
  • Material Science: In polymer chemistry, it acts as a building block for creating boron-containing polymers, which exhibit unique properties such as enhanced thermal stability and mechanical strength, making them suitable for advanced materials.
  • Environmental Chemistry: It plays a role in the remediation of environmental pollutants. Its ability to form complexes with heavy metals can be utilized in developing materials that capture and remove contaminants from water sources.

Citations