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Catalog Number:
40101
CAS Number:
380430-53-5
Acide 2-(éthoxycarbonyl)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-(éthoxycarbonyl)benzèneboronique
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Product Information

2-(Ethoxycarbonyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds. Its unique structure allows for the introduction of functional groups, facilitating the development of pharmaceuticals and agrochemicals. Researchers appreciate its stability and reactivity, which enhance its utility in various applications, including the synthesis of complex organic molecules and the development of targeted drug delivery systems.

In addition to its synthetic applications, 2-(Ethoxycarbonyl)phenylboronic acid has shown promise in the field of materials science, particularly in the creation of advanced polymers and nanomaterials. Its ability to form stable complexes with diols makes it valuable in sensor technology and catalysis. With its broad range of applications and the potential for innovation in various fields, this compound stands out as a crucial tool for researchers and industry professionals alike.

Synonyms
Acide 2-(éthoxycarbonyl)benzèneboronique
CAS Number
380430-53-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 9 H 11 BO 4
Molecular Weight
193.99
MDL Number
MFCD02179453
PubChem ID
2773405
Melting Point
138 °C (lit.)
Appearance
Poudre cristalline jaune clair à jaune
Conditions
Magasin chez RT
General Information
Synonyms
Acide 2-(éthoxycarbonyl)benzèneboronique
CAS Number
380430-53-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 9 H 11 BO 4
Molecular Weight
193.99
MDL Number
MFCD02179453
PubChem ID
2773405
Melting Point
138 °C (lit.)
Appearance
Poudre cristalline jaune clair à jaune
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-(Ethoxycarbonyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, allowing researchers to create complex carbon-carbon bonds efficiently, which is essential in drug discovery.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, enhancing the development of targeted therapies.
  • Sensor Development: This compound can be employed in the fabrication of chemical sensors due to its ability to selectively bind to certain biomolecules, aiding in environmental monitoring and medical diagnostics.
  • Material Science: It is also applied in the creation of advanced materials, such as polymers and nanomaterials, which can be utilized in electronics and catalysis, providing enhanced properties compared to traditional materials.

Citations