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Catalog Number:
40313
CAS Number:
900174-60-9
Ácido 5-etoxi-2-fluorofenilborónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 5-etoxi-2-fluorobencenoborónico
Documents
$79.22 /1G
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Product Information

5-Ethoxy-2-fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals can leverage its unique properties to develop novel pharmaceuticals and agrochemicals, enhancing the efficiency of synthetic pathways. The presence of the ethoxy group contributes to its solubility and reactivity, facilitating smoother reactions and higher yields compared to similar compounds.

In addition to its synthetic applications, 5-Ethoxy-2-fluorophenylboronic acid has shown potential in the development of targeted therapies, particularly in oncology, where boron-containing compounds are being explored for boron neutron capture therapy (BNCT). Its ability to selectively bind to specific biological targets opens avenues for innovative treatment strategies. With its favorable characteristics, this compound stands out as a key player in advancing research and development in various fields, making it an indispensable tool for chemists and researchers alike.

Synonyms
Ácido 5-etoxi-2-fluorobencenoborónico
CAS Number
900174-60-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 8 H 10 BFO3
Molecular Weight
183.97
MDL Number
MFCD05664321
PubChem ID
16217468
Melting Point
97 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 5-etoxi-2-fluorobencenoborónico
CAS Number
900174-60-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 8 H 10 BFO3
Molecular Weight
183.97
MDL Number
MFCD05664321
PubChem ID
16217468
Melting Point
97 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
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

5-Ethoxy-2-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its unique boronic acid functionality allows for selective reactions that are crucial in drug formulation.
  • Organic Synthesis: It is valuable in organic chemistry for cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for constructing complex organic molecules efficiently.
  • Material Science: The compound is used in creating advanced materials, including polymers and nanomaterials, due to its ability to form stable complexes with metals, enhancing material properties.
  • Bioconjugation: In biochemistry, it is employed for labeling biomolecules, facilitating the study of protein interactions and cellular processes, which is vital for understanding disease mechanisms.
  • Diagnostics: Its application extends to the development of diagnostic agents, where it can be used to create probes for imaging techniques, aiding in the early detection of diseases.

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