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Catalog Number:
40123
CAS Number:
179113-90-7
Acide 3-(trifluorométhoxy)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-(trifluorométhoxy)benzèneboronique
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Product Information

3-(Trifluoromethoxy)phenylboronic acid is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative features a trifluoromethoxy group, which enhances its reactivity and selectivity in various chemical reactions. It is particularly valuable in Suzuki coupling reactions, enabling the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules. Researchers and industry professionals utilize this compound to develop pharmaceuticals, agrochemicals, and advanced materials, making it an essential tool in modern chemistry.

The unique trifluoromethoxy substituent not only improves the compound's solubility in organic solvents but also contributes to its stability under various reaction conditions. This characteristic makes 3-(Trifluoromethoxy)phenylboronic acid an attractive choice for those looking to streamline their synthetic processes while achieving high yields. Its application in the development of novel drug candidates further underscores its importance in pharmaceutical research, where precision and efficiency are paramount.

Synonyms
Acide 3-(trifluorométhoxy)benzèneboronique
CAS Number
179113-90-7
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C7H6BF3O3
Molecular Weight
205.93
MDL Number
MFCD01320697
PubChem ID
2734385
Melting Point
89 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-(trifluorométhoxy)benzèneboronique
CAS Number
179113-90-7
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C7H6BF3O3
Molecular Weight
205.93
MDL Number
MFCD01320697
PubChem ID
2734385
Melting Point
89 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
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

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

  • Pharmaceutical Development: This compound plays a crucial role in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Its unique trifluoromethoxy group enhances the compound's reactivity and selectivity.
  • Organic Synthesis: It serves as a valuable building block in organic chemistry, enabling the formation of complex molecules through cross-coupling reactions. This application is particularly beneficial in creating compounds for agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings. Its properties can improve the durability and performance of these materials, making them suitable for various industrial applications.
  • Bioconjugation: In biochemistry, it is employed for labeling biomolecules, facilitating the study of protein interactions and cellular processes. This application is essential for researchers in the fields of molecular biology and biomedicine.
  • Environmental Chemistry: The compound is also investigated for its potential in environmental applications, such as the removal of pollutants from water sources. Its effectiveness in binding to certain contaminants makes it a candidate for developing new remediation technologies.

Citations