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Catalog Number:
40282
CAS Number:
73852-19-4
3,5-Bis(trifluoromethyl)phenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3,5-Bis(trifluoromethyl)benzeneboronic acid
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Product Information

3,5-Bis(trifluoromethyl)phenylboronic acid is a highly versatile compound known for its unique trifluoromethyl groups, which enhance its reactivity and solubility in various organic solvents. This boronic acid derivative is particularly valuable in the field of medicinal chemistry and materials science. It serves as a crucial building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its ability to form stable complexes with diols makes it an essential reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Researchers and industry professionals can leverage its properties for developing innovative materials, such as polymers and liquid crystals, as well as in the design of targeted drug delivery systems.

The compound's trifluoromethyl groups not only improve its electronic properties but also contribute to its stability under various conditions, making it an attractive choice for applications in high-performance materials. With its growing relevance in cutting-edge research and industrial applications, 3,5-Bis(trifluoromethyl)phenylboronic acid stands out as a key player in advancing chemical synthesis and material development.

Synonyms
3,5-Bis(trifluoromethyl)benzeneboronic acid
CAS Number
73852-19-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H5BF6O2
Molecular Weight
257.93
MDL Number
MFCD00051850
PubChem ID
156265
Melting Point
220 °C (Lit.)
Appearance
White to light orange to green powder
Conditions
Store at RT
General Information
Synonyms
3,5-Bis(trifluoromethyl)benzeneboronic acid
CAS Number
73852-19-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H5BF6O2
Molecular Weight
257.93
MDL Number
MFCD00051850
PubChem ID
156265
Melting Point
220 °C (Lit.)
Appearance
White to light orange to green 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

3,5-Bis(trifluoromethyl)phenylboronic acid is widely utilized in research focused on:

  • Drug Discovery: This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly in developing new treatments for cancer and other diseases.
  • Organic Electronics: It is used in the production of organic semiconductors, enhancing the performance of electronic devices such as OLEDs (Organic Light Emitting Diodes).
  • Catalysis: The compound acts as a catalyst in several chemical reactions, improving efficiency and selectivity in organic synthesis, which is crucial for the chemical industry.
  • Fluorinated Materials: Its unique trifluoromethyl groups contribute to the development of specialized materials with enhanced thermal and chemical stability, beneficial in coatings and polymers.
  • Analytical Chemistry: This boronic acid derivative is employed in sensor technology for detecting sugars and other biomolecules, aiding in medical diagnostics and environmental monitoring.

Citations