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Catalog Number:
40215
CAS Number:
900174-65-4
3-Ethoxy-4-fluorophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-Ethoxy-4-fluorobenzeneboronic acid
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Product Information

3-Ethoxy-4-fluorophenylboronic 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 Suzuki-Miyaura cross-coupling reactions. Its unique structure, featuring an ethoxy group and a fluorine atom, enhances its reactivity and selectivity, allowing for the efficient synthesis of complex organic molecules. Researchers and industry professionals can leverage this compound in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

In addition to its synthetic applications, 3-Ethoxy-4-fluorophenylboronic acid has shown potential in the field of targeted drug delivery and cancer therapy, where boron-containing compounds are being explored for their therapeutic benefits. Its favorable properties, such as solubility and stability, make it an attractive choice for researchers looking to innovate in drug design and development. With its broad range of applications and unique characteristics, this compound is a valuable addition to any laboratory focused on cutting-edge research and development.

Synonyms
3-Ethoxy-4-fluorobenzeneboronic acid
CAS Number
900174-65-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H10BFO3
Molecular Weight
183.97
MDL Number
MFCD09475831
PubChem ID
44558174
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Ethoxy-4-fluorobenzeneboronic acid
CAS Number
900174-65-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H10BFO3
Molecular Weight
183.97
MDL Number
MFCD09475831
PubChem ID
44558174
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

3-Ethoxy-4-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in the synthesis of various pharmaceuticals, particularly in creating targeted therapies for cancer treatment, enhancing drug efficacy through selective targeting.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, facilitating the formation of complex molecules through Suzuki coupling reactions, which are essential in developing new materials and chemicals.
  • Bioconjugation: The compound is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for developing diagnostic tools and therapeutic agents.
  • Material Science: In the field of material science, it is used to create advanced polymers and nanomaterials, improving properties like conductivity and strength, which are critical for electronics and structural applications.
  • Environmental Applications: It can be utilized in the development of sensors for detecting pollutants, contributing to environmental monitoring and protection efforts by providing sensitive and selective detection methods.

Citations