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Catalog Number:
40263
CAS Number:
874288-38-7
4-(Ethoxycarbonyl)-3-fluorophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-(Ethoxycarbonyl)-3-fluorobenzeneboronic acid
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Product Information

4-(Ethoxycarbonyl)-3-fluorophenylboronic acid is a versatile compound known for its unique properties that make it invaluable in various fields, particularly in organic synthesis and medicinal chemistry. This boronic acid derivative features a fluorine atom, which enhances its reactivity and selectivity in cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules. Its ability to form stable complexes with diols allows for applications in the development of sensors and catalysts, providing researchers with innovative tools for detecting and quantifying biological molecules.

In the pharmaceutical industry, 4-(Ethoxycarbonyl)-3-fluorophenylboronic acid is utilized in the synthesis of biologically active compounds, including potential drug candidates. Its unique structural characteristics facilitate the formation of diverse chemical entities, enabling the exploration of new therapeutic avenues. Researchers appreciate its compatibility with various reaction conditions, which enhances its utility in both academic and industrial settings. Overall, this compound stands out for its practical applications in synthesis and its potential to drive advancements in drug discovery and development.

Synonyms
4-(Ethoxycarbonyl)-3-fluorobenzeneboronic acid
CAS Number
874288-38-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H10BFO4
Molecular Weight
211.98
MDL Number
MFCD06656274
PubChem ID
2763245
Melting Point
161 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-(Ethoxycarbonyl)-3-fluorobenzeneboronic acid
CAS Number
874288-38-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H10BFO4
Molecular Weight
211.98
MDL Number
MFCD06656274
PubChem ID
2763245
Melting Point
161 °C (Lit.)
Appearance
White to off-white 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)-3-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its unique structure allows for targeted modifications that enhance therapeutic efficacy.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic compounds. This application is crucial for creating complex molecules in both academic and industrial settings.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules. This is particularly useful in drug delivery systems and diagnostic applications.
  • Fluorescent Probes: This chemical can be utilized in the design of fluorescent probes for biological imaging, enabling researchers to visualize cellular processes in real-time, which is vital for understanding disease mechanisms.

Citations