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Catalog Number:
40250
CAS Number:
133057-83-7
Ácido 4-benciloxi-3-fluorofenilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-benciloxi-3-fluorobencenoborónico
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Product Information

4-Benzyloxy-3-fluorophenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound 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 structure allows for selective functionalization, which is particularly beneficial in the synthesis of complex molecules. Researchers often utilize this compound in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create carbon-carbon bonds, thereby facilitating the construction of intricate organic frameworks.

In addition to its synthetic applications, 4-Benzyloxy-3-fluorophenylboronic acid has shown potential in the development of targeted therapies, particularly in the field of cancer research. Its ability to interact with specific biological targets can lead to the design of novel therapeutic agents. The compound's stability and reactivity make it a valuable tool for chemists and researchers looking to innovate in drug discovery and development. With its broad range of applications, this boronic acid derivative stands out as a key player in advancing chemical research and industrial applications.

Synonyms
Ácido 4-benciloxi-3-fluorobencenoborónico
CAS Number
133057-83-7
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C 13 H 12 BFO3
Molecular Weight
246.04
MDL Number
MFCD00994627
PubChem ID
2737788
Melting Point
131 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-benciloxi-3-fluorobencenoborónico
CAS Number
133057-83-7
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C 13 H 12 BFO3
Molecular Weight
246.04
MDL Number
MFCD00994627
PubChem ID
2737788
Melting Point
131 °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

4-Benzyloxy-3-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki reactions, which are essential for creating complex organic molecules used in agrochemicals and fine chemicals.
  • Material Science: The compound is used in the design of new materials, including polymers and nanomaterials, which can enhance properties like conductivity and strength.
  • Biochemistry: It acts as a tool for studying protein interactions and enzyme activities, helping researchers understand biological processes at a molecular level.
  • Diagnostics: This chemical is being explored for its potential in developing diagnostic agents that can selectively bind to specific biomolecules, improving disease detection methods.

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