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Catalog Number:
40275
CAS Number:
874219-35-9
4-Fluoro-3-(methoxycarbonyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Fluoro-3-(methoxycarbonyl)benzeneboronic acid
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Product Information

4-Fluoro-3-(methoxycarbonyl)phenylboronic 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 invaluable tool for the formation of carbon-carbon bonds. Its unique fluorine and methoxycarbonyl substituents enhance its reactivity and selectivity, allowing researchers to develop complex molecular architectures with precision.

In pharmaceutical research, 4-Fluoro-3-(methoxycarbonyl)phenylboronic acid is particularly useful in the synthesis of biologically active compounds, including potential drug candidates. Its application extends to the development of agrochemicals and materials science, where it aids in the creation of functionalized polymers and advanced materials. With its favorable properties, this compound stands out as a preferred choice for chemists seeking efficiency and effectiveness in their synthetic pathways.

Synonyms
4-Fluoro-3-(methoxycarbonyl)benzeneboronic acid
CAS Number
874219-35-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BFO4
Molecular Weight
197.96
MDL Number
MFCD06801688
PubChem ID
23005332
Melting Point
255 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Fluoro-3-(methoxycarbonyl)benzeneboronic acid
CAS Number
874219-35-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BFO4
Molecular Weight
197.96
MDL Number
MFCD06801688
PubChem ID
23005332
Melting Point
255 °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-(methoxycarbonyl)phenylboronic 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 boron-containing drugs that target specific biological pathways.
  • Organic Synthesis: It serves as an important building block in organic synthesis, allowing chemists to create complex molecules with enhanced properties, such as increased stability and reactivity.
  • Materials Science: The compound is used in developing advanced materials, including polymers and nanomaterials, which benefit from its unique chemical properties, leading to improved performance in applications like electronics and coatings.
  • Bioconjugation: It is utilized in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems and diagnostics.
  • Research in Catalysis: This chemical is employed in catalytic reactions, facilitating various transformations in organic chemistry, which can lead to more efficient and sustainable processes compared to traditional methods.

Citations