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Catalog Number:
40189
CAS Number:
248270-25-9
Acide 3-fluoro-4-formylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-fluoro-4-formylbenzèneboronique
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Product Information

3-Fluoro-4-formylphenylboronic acid is a versatile compound that plays a significant role 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 various complex organic molecules. Its unique fluorine substituent enhances the electronic properties of the compound, which can lead to improved reactivity and selectivity in chemical reactions. Researchers and industry professionals utilize this compound in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

In addition to its synthetic applications, 3-Fluoro-4-formylphenylboronic acid is also valuable in the field of bioconjugation and sensor development. Its boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it useful in the design of biosensors and drug delivery systems. The compound's ability to facilitate the creation of targeted therapies and diagnostic tools highlights its relevance in contemporary research and development. With its unique properties and practical applications, 3-Fluoro-4-formylphenylboronic acid stands out as a crucial component for innovative solutions in various scientific fields.

Synonyms
Acide 3-fluoro-4-formylbenzèneboronique
CAS Number
248270-25-9
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 7 H 6 BFO 3
Molecular Weight
167.93
MDL Number
MFCD02093051
PubChem ID
2778654
Melting Point
240 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-fluoro-4-formylbenzèneboronique
CAS Number
248270-25-9
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 7 H 6 BFO 3
Molecular Weight
167.93
MDL Number
MFCD02093051
PubChem ID
2778654
Melting Point
240 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
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

3-Fluoro-4-formylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its unique properties make it valuable in medicinal chemistry for designing new drugs, especially those targeting specific biological pathways.
  • Bioconjugation: The boronic acid functional group allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules in research.
  • Material Science: It is employed in the creation of advanced materials, including sensors and polymers, due to its ability to form stable complexes with various substrates.
  • Fluorine Chemistry: The presence of fluorine enhances the compound's reactivity and stability, making it a preferred choice in fluorine chemistry applications, including the development of fluorinated compounds.