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Catalog Number:
27553
CAS Number:
1765-93-1
Ácido 4-fluorofenilborónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
(4-Fluorofenil)boranediol
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Product Information

4-Fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique fluorine substitution enhances its reactivity and selectivity in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, which is pivotal for constructing complex organic molecules. Researchers appreciate its role in the synthesis of biologically active compounds, including potential anti-cancer agents and other therapeutic drugs.

In addition to its applications in drug discovery, 4-Fluorophenylboronic acid is also employed in the development of sensors and materials science, where its boron functionality can be leveraged for creating advanced materials with tailored properties. Its compatibility with a range of solvents and stability under various conditions further underscores its utility in both laboratory and industrial settings. By integrating this compound into your research or production processes, you can enhance the efficiency and effectiveness of your synthetic methodologies.

Synonyms
(4-Fluorofenil)boranediol
CAS Number
1765-93-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C6H6BFO2
Molecular Weight
139.92
MDL Number
MFCD00039136
PubChem ID
285645
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(4-Fluorofenil)boranediol
CAS Number
1765-93-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C6H6BFO2
Molecular Weight
139.92
MDL Number
MFCD00039136
PubChem ID
285645
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-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 drugs targeting cancer and other diseases. Its ability to form stable complexes with certain biomolecules enhances drug efficacy.
  • Organic Synthesis: It is commonly used in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic molecules. This application is crucial in the production of agrochemicals and fine chemicals.
  • Material Science: The compound plays a significant role in the development of advanced materials, including polymers and nanomaterials. Its unique properties allow for the creation of materials with specific functionalities, beneficial in electronics and coatings.
  • Bioconjugation: 4-Fluorophenylboronic acid is utilized in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules. This is particularly useful in biosensors and diagnostic applications.
  • Research in Chemical Biology: It is employed in the study of cellular processes and enzyme interactions, providing insights into biological mechanisms. This application is vital for researchers exploring new therapeutic targets.

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