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Catalog Number:
40239
CAS Number:
156545-07-2
Acide 3,5-difluorophénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 3,5-difluorobenzèneboronique
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Product Information

3,5-Difluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its unique ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its distinct fluorine substituents enhance its reactivity and selectivity, allowing for more efficient coupling reactions in the synthesis of complex organic molecules. Researchers have successfully employed 3,5-Difluorophenylboronic acid in the preparation of biologically active compounds, including potential anti-cancer agents and other therapeutic molecules, showcasing its relevance in drug discovery and development.

In addition to its applications in pharmaceuticals, this compound is also valuable in materials science, particularly in the development of advanced polymers and sensors. Its ability to participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, makes it a preferred choice for creating functionalized materials with tailored properties. The compound's stability and ease of handling further enhance its appeal for both academic and industrial applications, positioning it as a key player in innovative research and development projects.

Synonyms
Acide 3,5-difluorobenzèneboronique
CAS Number
156545-07-2
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C6H5BF2O2
Molecular Weight
157.91
MDL Number
MFCD01318138
PubChem ID
2734338
Melting Point
250 °C (lit.)
Appearance
Poudre cristalline blanche à orange
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3,5-difluorobenzèneboronique
CAS Number
156545-07-2
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C6H5BF2O2
Molecular Weight
157.91
MDL Number
MFCD01318138
PubChem ID
2734338
Melting Point
250 °C (lit.)
Appearance
Poudre cristalline blanche à orange
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

3,5-Difluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in synthesizing various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases. Its unique properties allow for the creation of more effective therapeutic agents.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, facilitating the formation of complex molecules. Researchers leverage its boronic acid functionality for coupling reactions, enhancing the efficiency of synthetic pathways.
  • Materials Science: The compound is used in creating advanced materials, including polymers and nanomaterials. Its ability to form stable bonds makes it valuable in developing materials with specific properties for electronics and coatings.
  • Bioconjugation: In biochemistry, it is utilized for attaching biomolecules to surfaces or other molecules, aiding in the development of biosensors and drug delivery systems. This application is vital for improving the efficacy of therapeutic interventions.
  • Fluorescent Probes: The compound can be incorporated into fluorescent probes for imaging applications in biological research. This allows scientists to visualize cellular processes in real-time, providing insights into disease mechanisms.

Citations