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Catalog Number:
40211
CAS Number:
279263-10-4
4-Ethoxy-3-fluorophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Ethoxy-3-fluorobenzeneboronic acid
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Product Information

4-Ethoxy-3-fluorophenylboronic acid is a versatile organoboron compound that plays a significant role in various fields, particularly in medicinal chemistry and organic synthesis. This compound is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of boron-based catalysts and in Suzuki-Miyaura cross-coupling reactions. Its unique structure, featuring both an ethoxy group and a fluorine atom, enhances its reactivity and selectivity, allowing for precise modifications in complex organic molecules.

Researchers and industry professionals can leverage 4-Ethoxy-3-fluorophenylboronic acid in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its application in the preparation of biologically active compounds highlights its importance in drug discovery and development. Additionally, the compound's compatibility with various reaction conditions makes it a valuable tool for chemists looking to streamline their synthetic pathways. With its unique properties and practical applications, this boronic acid derivative stands out as a key ingredient in modern chemical research and industrial processes.

Synonyms
4-Ethoxy-3-fluorobenzeneboronic acid
CAS Number
279263-10-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H10BFO3
Molecular Weight
183.97
MDL Number
MFCD04115667
PubChem ID
2782821
Melting Point
113 °C (Lit.)
Appearance
White to off white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Ethoxy-3-fluorobenzeneboronic acid
CAS Number
279263-10-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H10BFO3
Molecular Weight
183.97
MDL Number
MFCD04115667
PubChem ID
2782821
Melting Point
113 °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-Ethoxy-3-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is instrumental in the synthesis of various pharmaceuticals, particularly in creating targeted therapies for cancer treatment.
  • Organic Synthesis: It serves as a key building block in organic chemistry, facilitating the formation of complex molecules through Suzuki coupling reactions.
  • Material Science: The compound is used in developing advanced materials, including polymers and coatings, enhancing their properties such as durability and chemical resistance.
  • Bioconjugation: It plays a significant role in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial for drug delivery systems.
  • Diagnostic Applications: The compound is utilized in the development of diagnostic agents, improving the sensitivity and specificity of detection methods in clinical settings.

Citations