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Catalog Number:
45852
CAS Number:
65295-58-1
Bromuro de 3-(4-fluorofenoxi)bencilo
Purity:
≥ 97% (GC)
Synonym(s):
Éter de 3'-bromometil-4-fluorodifenilo
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Product Information

3-(4-Fluorophenoxy)benzyl bromide is a versatile chemical compound that serves as a crucial intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound is recognized for its unique reactivity, which allows it to participate in various coupling reactions, making it an essential building block for creating complex molecular structures. Its fluorophenyl group enhances its lipophilicity, which can improve the bioavailability of drug candidates, making it particularly valuable in medicinal chemistry.

In addition to its applications in drug discovery, 3-(4-Fluorophenoxy)benzyl bromide is also utilized in the synthesis of advanced materials and functional polymers. Researchers appreciate its ability to facilitate the introduction of fluorine into organic molecules, which can significantly alter the physical and chemical properties of the resulting compounds. This characteristic is particularly beneficial in the development of materials with enhanced thermal stability and chemical resistance. With its broad range of applications, this compound is an indispensable tool for professionals in the fields of pharmaceuticals, materials science, and chemical research.

Synonyms
Éter de 3'-bromometil-4-fluorodifenilo
CAS Number
65295-58-1
Purity
≥ 97% (GC)
Molecular Formula
C13H10BrFO
Molecular Weight
281.12
MDL Number
MFCD00059915
PubChem ID
2737456
Appearance
Polvo de color blanco a naranja a verde en grumos
Boiling Point
160 °C/2,3 mmHg
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Éter de 3'-bromometil-4-fluorodifenilo
CAS Number
65295-58-1
Purity
≥ 97% (GC)
Molecular Formula
C13H10BrFO
Molecular Weight
281.12
MDL Number
MFCD00059915
PubChem ID
2737456
Appearance
Polvo de color blanco a naranja a verde en grumos
Boiling Point
160 °C/2,3 mmHg
Conditions
Conservar entre 2 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

3-(4-Fluorophenoxy)benzyl bromide is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders, due to its ability to modify biological activity.
  • Development of Agrochemicals: It is employed in the formulation of agrochemicals, enhancing the efficacy of herbicides and pesticides by improving their penetration and effectiveness on plant surfaces.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, where its unique properties contribute to improved durability and resistance to environmental factors.
  • Bioconjugation Techniques: In biochemistry, it is utilized for bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, facilitating studies in drug delivery and diagnostics.
  • Fluorescent Probes: This chemical is also used in the creation of fluorescent probes for imaging applications in biological research, providing valuable insights into cellular processes and interactions.

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