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Catalog Number:
40213
CAS Number:
825644-26-6
4-Fluoro-2-formylphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
4-Fluoro-2-formylbenzeneboronic acid
Documents
$140.11 /1G
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Product Information

4-Fluoro-2-formylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued 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 substitution enhances its reactivity and selectivity, allowing for more efficient coupling processes compared to other boronic acids.

In addition to its synthetic applications, 4-Fluoro-2-formylphenylboronic acid serves as a crucial intermediate in the development of targeted therapies, particularly in the field of cancer research. Researchers appreciate its compatibility with various functional groups, enabling the creation of diverse molecular architectures. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, making it an ideal choice for both academic and industrial applications.

Synonyms
4-Fluoro-2-formylbenzeneboronic acid
CAS Number
825644-26-6
Purity
≥ 98% (HPLC)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD10697426
PubChem ID
25185241
Melting Point
125 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Fluoro-2-formylbenzeneboronic acid
CAS Number
825644-26-6
Purity
≥ 98% (HPLC)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD10697426
PubChem ID
25185241
Melting Point
125 °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-2-formylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs and crop protection agents.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it valuable in bioconjugation techniques for labeling biomolecules, which is essential in drug delivery systems.
  • Fluorescent Probes: The compound can be used to create fluorescent probes for biological imaging, helping researchers visualize cellular processes in real-time.
  • Material Science: It is applied in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and mechanical strength.
  • Chemical Sensors: The unique reactivity of this compound allows for the design of chemical sensors that can detect specific biomolecules, aiding in diagnostics and environmental monitoring.

Citations