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Catalog Number:
40207
CAS Number:
855230-61-4
3-Ethoxy-2-fluorophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3-Ethoxy-2-fluorobenzeneboronic acid
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Product Information

3-Ethoxy-2-fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized 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, featuring a fluorine atom and an ethoxy group, enhances its reactivity and selectivity, allowing for the development of targeted compounds with improved efficacy.

Researchers and industry professionals can leverage 3-Ethoxy-2-fluorophenylboronic acid in the design of novel drug candidates, particularly in the development of anti-cancer agents and other therapeutic compounds. Its compatibility with various reaction conditions and functional groups makes it a valuable tool in the synthesis of biologically active molecules. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, ensuring reliable results in synthetic applications.

Synonyms
3-Ethoxy-2-fluorobenzeneboronic acid
CAS Number
855230-61-4
Purity
98 - 105% (Assay by titration)
Molecular Formula
C8H10BFO3
Molecular Weight
183.97
MDL Number
MFCD06798077
PubChem ID
16217759
Melting Point
83 °C (Lit.)
Appearance
White to off white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Ethoxy-2-fluorobenzeneboronic acid
CAS Number
855230-61-4
Purity
98 - 105% (Assay by titration)
Molecular Formula
C8H10BFO3
Molecular Weight
183.97
MDL Number
MFCD06798077
PubChem ID
16217759
Melting Point
83 °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

3-Ethoxy-2-fluorophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in the synthesis of pharmaceutical agents, particularly in the development of targeted therapies for cancer treatment.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, facilitating the formation of complex molecules through cross-coupling reactions.
  • Material Science: The compound is used in the creation of advanced materials, including polymers and coatings, which benefit from its unique chemical properties.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools.
  • Fluorescent Probes: This chemical can be utilized in the development of fluorescent probes for imaging applications, aiding in biological research and diagnostics.

Citations