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Catalog Number:
40252
CAS Number:
5785-70-6
4-Ethoxycarbonyl-2-nitrophenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
4-Ethoxycarbonyl-2-nitrobenzeneboronic acid
Documents
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Product Information

4-Ethoxycarbonyl-2-nitrophenylboronic acid is a versatile compound that plays a crucial role in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure allows for selective reactivity, which is beneficial in the development of targeted therapies and advanced materials. Researchers appreciate its stability and compatibility with various functional groups, enabling the creation of diverse chemical architectures.

In addition to its synthetic applications, 4-Ethoxycarbonyl-2-nitrophenylboronic acid has potential uses in the development of sensors and catalysts due to its ability to form reversible complexes with diols. This characteristic opens avenues for innovative applications in environmental monitoring and chemical sensing. The compound's favorable properties make it a valuable asset for both academic research and industrial applications, providing a reliable option for professionals seeking to enhance their chemical processes.

Synonyms
4-Ethoxycarbonyl-2-nitrobenzeneboronic acid
CAS Number
5785-70-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H10BNO6
Molecular Weight
238.99
MDL Number
MFCD02179460
PubChem ID
2773403
Melting Point
125 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Ethoxycarbonyl-2-nitrobenzeneboronic acid
CAS Number
5785-70-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H10BNO6
Molecular Weight
238.99
MDL Number
MFCD02179460
PubChem ID
2773403
Melting Point
125 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at 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-2-nitrophenylboronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile building block in organic synthesis, particularly in the formation of complex molecules, making it invaluable for chemists developing new pharmaceuticals.
  • Medicinal Chemistry: It plays a crucial role in the design of boron-containing drugs, which can enhance the efficacy of treatments for various diseases, including cancer, by targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in the development of targeted drug delivery systems.
  • Fluorescent Probes: Its unique properties make it suitable for creating fluorescent probes, which are used in imaging techniques to study biological processes in real-time.
  • Environmental Chemistry: This chemical is applied in the detection and remediation of pollutants, helping to develop methods for monitoring environmental contaminants effectively.

Citations