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Catalog Number:
40110
CAS Number:
4334-87-6
Acide 3-(éthoxycarbonyl)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-(éthoxycarbonyl)benzèneboronique
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Product Information

3-(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 form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for the introduction of various functional groups, facilitating the development of complex molecules in pharmaceuticals and agrochemicals. Researchers appreciate its role in the synthesis of biologically active compounds, including potential drug candidates and intermediates.

In addition to its synthetic applications, 3-(Ethoxycarbonyl)phenylboronic acid exhibits significant potential in materials science, particularly in the development of sensors and polymers. Its ability to interact with specific biomolecules opens avenues for applications in biosensing and targeted drug delivery systems. The compound's stability and ease of handling make it an attractive choice for both laboratory and industrial settings, providing researchers with a reliable tool for advancing their projects.

Synonyms
Acide 3-(éthoxycarbonyl)benzèneboronique
CAS Number
4334-87-6
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 9 H 11 BO 4
Molecular Weight
193.99
MDL Number
MFCD02179444
PubChem ID
3249312
Melting Point
138 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-(éthoxycarbonyl)benzèneboronique
CAS Number
4334-87-6
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 9 H 11 BO 4
Molecular Weight
193.99
MDL Number
MFCD02179444
PubChem ID
3249312
Melting Point
138 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
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

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

  • Organic Synthesis: This compound is a valuable building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic structures.
  • Drug Development: Researchers leverage its properties to create new drug candidates, particularly in the field of cancer treatment, due to its ability to modify biological targets effectively.
  • Material Science: The compound is used in the production of advanced materials, including polymers and nanomaterials, enhancing their functional properties.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other compounds, which is vital in diagnostics and therapeutic applications.

Citations