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Catalog Number:
31435
CAS Number:
139301-27-2
4-(Trifluoromethoxy)phenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
4-(Trifluoromethoxy)benzeneboronic acid
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Product Information

4-(Trifluoromethoxy)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds. Its trifluoromethoxy group enhances its reactivity and solubility, allowing for efficient coupling with a variety of electrophiles. Researchers and industry professionals appreciate its role in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

In addition to its synthetic applications, 4-(Trifluoromethoxy)phenylboronic acid has shown promise in the field of diagnostics and sensor technology due to its unique chemical properties. Its ability to form stable complexes with various substrates opens avenues for innovative applications in biosensing and environmental monitoring. By incorporating this compound into their research, professionals can enhance the efficacy and specificity of their projects, paving the way for groundbreaking discoveries.

Synonyms
4-(Trifluoromethoxy)benzeneboronic acid
CAS Number
139301-27-2
Purity
≥ 99% (HPLC)
Molecular Formula
C7H6BF3O3
Molecular Weight
205.93
MDL Number
MFCD01074648
PubChem ID
2734386
Melting Point
120 - 130 ?C
Appearance
White to off-white powder
Conditions
Store at RT
General Information
Synonyms
4-(Trifluoromethoxy)benzeneboronic acid
CAS Number
139301-27-2
Purity
≥ 99% (HPLC)
Molecular Formula
C7H6BF3O3
Molecular Weight
205.93
MDL Number
MFCD01074648
PubChem ID
2734386
Melting Point
120 - 130 ?C
Appearance
White to off-white powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(Trifluoromethoxy)phenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial intermediate in synthesizing pharmaceuticals, particularly in developing treatments for cancer and other diseases, due to its ability to form stable complexes with various biomolecules.
  • Organic Synthesis: It is employed in cross-coupling reactions, which are essential for constructing complex organic molecules. This application is particularly valuable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in creating advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings, enhancing durability and performance.
  • Analytical Chemistry: It acts as a reagent in various analytical techniques, including chromatography and spectroscopy, helping researchers detect and quantify compounds with high precision.
  • Environmental Chemistry: This chemical is utilized in studying the behavior of pollutants and developing methods for environmental remediation, contributing to cleaner ecosystems and sustainable practices.

Citations