Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
28090
CAS Number:
1423-26-3
Ácido 3-(trifluorometil)fenilborónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 3-trifluorometilborónico, 3-Boronobenzotrifluoruro
Documents
$22.03 /5G
Tamaño
Request Bulk Quote
Product Information

3-(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 chemical reactions, particularly in Suzuki coupling reactions. Researchers and industry professionals leverage this compound for the development of pharmaceuticals, agrochemicals, and advanced materials, making it an essential building block in the synthesis of complex organic molecules. Its ability to form stable complexes with diols also makes it valuable in sensor applications and in the development of boron-containing materials.

The compound's distinctive properties, such as its high thermal stability and solubility in organic solvents, further enhance its appeal for laboratory and industrial applications. With its increasing relevance in the fields of drug discovery and materials science, 3-(Trifluoromethyl)phenylboronic acid stands out as a crucial reagent for innovative research and development projects, providing significant advantages over similar compounds in terms of efficiency and specificity.

Synonyms
Ácido 3-trifluorometilborónico, 3-Boronobenzotrifluoruro
CAS Number
1423-26-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C7H6BF3O2
Molecular Weight
189.93
MDL Number
MFCD00151854
PubChem ID
2734388
Melting Point
158-169 ?C
Appearance
Sólido de color blanquecino a tostado
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 3-trifluorometilborónico, 3-Boronobenzotrifluoruro
CAS Number
1423-26-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C7H6BF3O2
Molecular Weight
189.93
MDL Number
MFCD00151854
PubChem ID
2734388
Melting Point
158-169 ?C
Appearance
Sólido de color blanquecino a tostado
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(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.
  • Chemical Reactions: It is commonly used in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds.
  • Material Science: The compound is applied in the development of advanced materials, including polymers and coatings, enhancing properties such as thermal stability and chemical resistance.
  • Bioconjugation: It plays a significant role in bioconjugation strategies, allowing researchers to attach biomolecules to surfaces or other compounds, facilitating drug delivery and diagnostic applications.
  • Fluorinated Compounds: The trifluoromethyl group enhances the biological activity and lipophilicity of compounds, making it valuable in medicinal chemistry for improving drug efficacy.

Citas