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Catalog Number:
40230
CAS Number:
85107-55-7
4-(Methoxycarbonyl)-2-nitrophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-(Methoxycarbonyl)-2-nitrobenzeneboronic acid
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Product Information

4-(Methoxycarbonyl)-2-nitrophenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Researchers appreciate its role in the synthesis of biologically active compounds, including potential drug candidates and advanced materials.

The compound's properties, such as its moderate solubility in organic solvents and stability under standard laboratory conditions, enhance its applicability in diverse research environments. Its effectiveness in facilitating the formation of carbon-carbon bonds positions it as a valuable tool for chemists aiming to innovate in drug discovery and materials science. With its proven track record in enhancing reaction efficiency and selectivity, 4-(Methoxycarbonyl)-2-nitrophenylboronic acid stands out as a key reagent for professionals seeking to advance their projects in synthetic chemistry.

Synonyms
4-(Methoxycarbonyl)-2-nitrobenzeneboronic acid
CAS Number
85107-55-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BNO6
Molecular Weight
224.96
MDL Number
MFCD01632202
PubChem ID
2773493
Melting Point
168 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-(Methoxycarbonyl)-2-nitrobenzeneboronic acid
CAS Number
85107-55-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BNO6
Molecular Weight
224.96
MDL Number
MFCD01632202
PubChem ID
2773493
Melting Point
168 °C (Lit.)
Appearance
White to light 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-(Methoxycarbonyl)-2-nitrophenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its unique properties make it valuable in medicinal chemistry for designing and optimizing drug candidates, especially those targeting specific biological pathways.
  • Bioconjugation: The compound is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other compounds, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Fluorescent Probes: It can be used to create fluorescent probes for imaging applications in biological research, aiding in the visualization of cellular processes.
  • Environmental Monitoring: This chemical is also applied in environmental chemistry for detecting and quantifying pollutants, contributing to efforts in environmental protection and sustainability.

Citations