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Catalog Number:
40213
CAS Number:
825644-26-6
Acide 4-fluoro-2-formylphénylboronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 4-fluoro-2-formylbenzèneboronique
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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
Acide 4-fluoro-2-formylbenzèneboronique
CAS Number
825644-26-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 7 H 6 BFO 3
Molecular Weight
167.93
MDL Number
MFCD10697426
PubChem ID
25185241
Melting Point
125 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-fluoro-2-formylbenzèneboronique
CAS Number
825644-26-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 7 H 6 BFO 3
Molecular Weight
167.93
MDL Number
MFCD10697426
PubChem ID
25185241
Melting Point
125 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
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