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Catalog Number:
40095
CAS Number:
9 de marzo de 1993
Ácido 2-fluorofenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 2-fluorobencenoborónico
Documents
$35.15 /1G
Tamaño
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Product Information

2-Fluorophenylboronic acid is a versatile organoboron compound recognized for its significant role in organic synthesis and medicinal chemistry. This compound features a fluorine atom on the aromatic ring, enhancing its reactivity and selectivity in various chemical reactions. It is commonly utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal for constructing complex biaryl compounds. These biaryl structures are essential in the development of pharmaceuticals, agrochemicals, and advanced materials.

Moreover, 2-Fluorophenylboronic acid serves as a valuable building block in the synthesis of fluorescent probes and sensors, making it a preferred choice for researchers in the fields of biochemistry and materials science. Its unique properties, such as the ability to form stable complexes with diols, further expand its application in the development of targeted drug delivery systems and diagnostic tools. With its broad utility and effectiveness, 2-Fluorophenylboronic acid stands out as a crucial reagent for professionals aiming to innovate in chemical research and development.

Synonyms
Ácido 2-fluorobencenoborónico
CAS Number
9 de marzo de 1993
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C6H6BFO2
Molecular Weight
139.92
MDL Number
MFCD00674013
PubChem ID
2734354
Melting Point
110 °C (Literatura)
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 2-fluorobencenoborónico
CAS Number
9 de marzo de 1993
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C6H6BFO2
Molecular Weight
139.92
MDL Number
MFCD00674013
PubChem ID
2734354
Melting Point
110 °C (Literatura)
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Fluorophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound is essential in synthesizing pharmaceuticals, particularly in creating targeted therapies for cancer, due to its ability to form stable bonds with biomolecules.
  • Organic Synthesis: It serves as a key reagent in cross-coupling reactions, enabling chemists to construct complex organic molecules efficiently, which is crucial in developing new materials and chemicals.
  • Bioconjugation: The unique properties of this boronic acid allow for selective binding to diols in biomolecules, making it valuable in the design of drug delivery systems and biosensors.
  • Material Science: It is used in the development of advanced materials, such as polymers and coatings, that require specific functional properties, enhancing performance in various applications.
  • Analytical Chemistry: This compound is employed in analytical techniques to detect and quantify specific biomolecules, providing researchers with critical data for various studies.

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