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Catalog Number:
40335
CAS Number:
182482-25-3
2,4,6-Trifluorophenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2,4,6-Trifluorobenzeneboronic acid
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$33.75 /1G
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Product Information

2,4,6-Trifluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its unique trifluoromethyl group, which enhances its reactivity and selectivity in various chemical reactions. It serves as a crucial building block in the development of pharmaceuticals, agrochemicals, and advanced materials. Researchers often employ 2,4,6-Trifluorophenylboronic acid in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds essential for constructing complex molecular architectures. Its ability to form stable complexes with diols also makes it valuable in sensor technology and the development of boron-based catalysts.

The compound's distinctive properties, including its high solubility in organic solvents and compatibility with a range of functional groups, make it an attractive choice for chemists seeking efficient and effective solutions in their synthetic pathways. With its growing importance in the field of drug discovery and materials science, 2,4,6-Trifluorophenylboronic acid stands out as a key reagent that can significantly enhance the efficiency of chemical processes.

Synonyms
2,4,6-Trifluorobenzeneboronic acid
CAS Number
182482-25-3
Purity
≥ 98% (HPLC)
Molecular Formula
C6H4BF3O2
Molecular Weight
175.9
MDL Number
MFCD01863169
PubChem ID
2779329
Melting Point
235 °C (Lit.)
Appearance
White to off-white powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2,4,6-Trifluorobenzeneboronic acid
CAS Number
182482-25-3
Purity
≥ 98% (HPLC)
Molecular Formula
C6H4BF3O2
Molecular Weight
175.9
MDL Number
MFCD01863169
PubChem ID
2779329
Melting Point
235 °C (Lit.)
Appearance
White to off-white powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,4,6-Trifluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is instrumental in the synthesis of various pharmaceuticals, particularly in creating boron-containing drugs that can enhance therapeutic efficacy.
  • Organic Synthesis: It serves as a key reagent in Suzuki coupling reactions, allowing chemists to form carbon-carbon bonds efficiently, which is crucial for building complex organic molecules.
  • Material Science: The compound is used in the development of new materials, including polymers and nanomaterials, due to its unique electronic properties and ability to modify surfaces.
  • Fluorescent Probes: Researchers utilize it to create fluorescent probes for biological imaging, helping to visualize cellular processes in real-time, which is vital for understanding disease mechanisms.
  • Environmental Chemistry: It is applied in the detection and analysis of environmental pollutants, aiding in the development of sensors that can monitor water quality and other ecological parameters.

Citations