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Catalog Number:
40098
CAS Number:
1423-27-4
Acide 2-(trifluorométhyl)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide α,alpha,alpha-trifluoro- o -toluèneboronique, Acide α,α,α-trifluoro -o -tolylboronique
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Product Information

2-(Trifluoromethyl)phenylboronic 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 coupling reactions, such as Suzuki-Miyaura cross-coupling. Researchers and industry professionals leverage this compound for the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount. Its ability to form stable complexes with diols makes it particularly valuable in the synthesis of complex organic molecules, enabling the creation of innovative products with enhanced properties.

In addition to its synthetic applications, 2-(Trifluoromethyl)phenylboronic acid serves as a crucial building block in the design of fluorescent probes and sensors, contributing to advancements in analytical chemistry. The compound's distinctive properties, including its high stability and solubility in various solvents, make it an ideal choice for researchers seeking reliable and effective reagents. By incorporating this compound into their workflows, professionals can achieve greater yields and improved outcomes in their projects, ultimately driving innovation in their respective fields.

Synonyms
Acide α,alpha,alpha-trifluoro- o -toluèneboronique, Acide α,α,α-trifluoro -o -tolylboronique
CAS Number
1423-27-4
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C7H6BF3O2
Molecular Weight
189.93
MDL Number
MFCD00236059
PubChem ID
2734387
Melting Point
111 - 114 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide α,alpha,alpha-trifluoro- o -toluèneboronique, Acide α,α,α-trifluoro -o -tolylboronique
CAS Number
1423-27-4
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C7H6BF3O2
Molecular Weight
189.93
MDL Number
MFCD00236059
PubChem ID
2734387
Melting Point
111 - 114 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-(Trifluoromethyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique trifluoromethyl group enhances the biological activity of the resulting compounds.
  • Chemical Reactions: It is commonly used in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds. This application is crucial in the production of complex organic compounds in the pharmaceutical industry.
  • Material Science: The compound is applied in the development of advanced materials, including polymers and coatings. Its properties allow for improved performance in terms of durability and chemical resistance.
  • Medicinal Chemistry: Researchers utilize this boronic acid in the design of inhibitors for various enzymes, particularly proteases. Its ability to form reversible covalent bonds makes it a valuable tool in drug discovery.
  • Analytical Chemistry: It is employed in the development of sensors and analytical methods for detecting specific biomolecules, enhancing the sensitivity and selectivity of assays in clinical diagnostics.

Citations