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Catalog Number:
40192
CAS Number:
854778-31-7
4-Fluoro-3-methoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Fluoro-3-methoxybenzeneboronic acid
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Product Information

4-Fluoro-3-methoxyphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound 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 fluorine and methoxy substituents enhance its reactivity and selectivity, allowing for the development of targeted compounds with improved efficacy and reduced side effects.

Researchers and industry professionals can leverage 4-Fluoro-3-methoxyphenylboronic acid in the design of novel drug candidates, particularly in the field of cancer therapy and other therapeutic areas where precision is paramount. Its compatibility with various reaction conditions and ease of handling make it a preferred choice for laboratories focused on innovative chemical synthesis. With its proven track record in facilitating the creation of valuable compounds, this boronic acid derivative stands out as a key reagent for advancing research and development in multiple sectors.

Synonyms
4-Fluoro-3-methoxybenzeneboronic acid
CAS Number
854778-31-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD08056358
PubChem ID
44558185
Melting Point
191 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Fluoro-3-methoxybenzeneboronic acid
CAS Number
854778-31-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD08056358
PubChem ID
44558185
Melting Point
191 °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-Fluoro-3-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura reactions, which are essential for creating complex organic molecules in the chemical industry.
  • Materials Science: The compound is used in the fabrication of advanced materials, including polymers and nanomaterials, enhancing their properties for applications in electronics and coatings.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, aiding in the attachment of biomolecules to surfaces or other molecules, which is vital in drug delivery systems.
  • Analytical Chemistry: This chemical is utilized in various analytical methods, including chromatography and spectroscopy, for the detection and quantification of other compounds in complex mixtures.

Citations