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Catalog Number:
40096
CAS Number:
4334-88-7
Ácido 4-(etoxicarbonil)fenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-(etoxicarbonil)bencenoborónico
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Product Information

4-(Ethoxycarbonyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and pharmaceutical research. 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 often leverage its unique properties to facilitate the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its application in the development of targeted therapies highlights its significance in medicinal chemistry, particularly in the creation of compounds that can selectively interact with biological targets.

Additionally, 4-(Ethoxycarbonyl)phenylboronic acid serves as a valuable building block in the synthesis of various functional materials and polymers. Its compatibility with diverse reaction conditions enhances its utility in both academic and industrial settings. By incorporating this compound into their workflows, chemists can streamline their processes and achieve higher yields in their synthetic endeavors. With its robust performance and adaptability, 4-(Ethoxycarbonyl)phenylboronic acid stands out as a key player in modern chemical research and development.

Synonyms
Ácido 4-(etoxicarbonil)bencenoborónico
CAS Number
4334-88-7
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C 9 H 11 BO 4
Molecular Weight
193.99
MDL Number
MFCD02179441
PubChem ID
2734350
Melting Point
160 °C (descenso)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-(etoxicarbonil)bencenoborónico
CAS Number
4334-88-7
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C 9 H 11 BO 4
Molecular Weight
193.99
MDL Number
MFCD02179441
PubChem ID
2734350
Melting Point
160 °C (descenso)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(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 plays a crucial role in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic structures.
  • Drug Development: The compound is used in the design of boron-containing drugs, offering unique properties that enhance the efficacy and selectivity of therapeutic agents.
  • Material Science: It is applied in the creation of functionalized polymers and materials, contributing to advancements in electronics and nanotechnology.
  • Bioconjugation: This chemical is utilized in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital in diagnostics and therapeutic applications.

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