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Catalog Number:
40267
CAS Number:
153254-09-2
Acide 2,4-bis(trifluorométhyl)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2,4-bis(trifluorométhyl)benzèneboronique
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Product Information

2,4-Bis(trifluoromethyl)phenylboronic acid is a highly specialized compound known for its unique trifluoromethyl groups that enhance its reactivity and selectivity in various chemical reactions. This boronic acid derivative is particularly valuable in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with diols makes it an essential reagent in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Researchers and industry professionals utilize this compound to facilitate the synthesis of biologically active compounds, contributing to advancements in medicinal chemistry.

Moreover, 2,4-Bis(trifluoromethyl)phenylboronic acid exhibits excellent solubility in organic solvents, making it an ideal choice for various laboratory applications. Its unique properties allow for enhanced reaction rates and yields, providing significant advantages over similar compounds. This makes it a preferred reagent for chemists looking to optimize their synthetic pathways. With its broad applicability in research and industry, this compound stands out as a crucial tool for those engaged in cutting-edge chemical synthesis.

Synonyms
Acide 2,4-bis(trifluorométhyl)benzèneboronique
CAS Number
153254-09-2
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C8H5BF6O2
Molecular Weight
257.93
MDL Number
MFCD01631349
PubChem ID
2782667
Melting Point
110 - 117 °C
Appearance
Poudre cristalline blanche à légèrement jaune
Conditions
Magasin chez RT
General Information
Synonyms
Acide 2,4-bis(trifluorométhyl)benzèneboronique
CAS Number
153254-09-2
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C8H5BF6O2
Molecular Weight
257.93
MDL Number
MFCD01631349
PubChem ID
2782667
Melting Point
110 - 117 °C
Appearance
Poudre cristalline blanche à légèrement jaune
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

2,4-Bis(trifluoromethyl)phenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is instrumental in synthesizing various pharmaceuticals, particularly in the creation of boronic acid derivatives that are key in drug discovery and development.
  • Organic Synthesis: It serves as a crucial reagent in cross-coupling reactions, allowing chemists to construct complex organic molecules efficiently, which is essential in materials science and agrochemicals.
  • Fluorinated Materials: The trifluoromethyl groups enhance the properties of materials, making them more hydrophobic and thermally stable, which is beneficial in the production of high-performance coatings and polymers.
  • Bioconjugation: Its unique structure allows for effective bioconjugation techniques, making it valuable in the development of targeted therapies and diagnostic tools in biotechnology.
  • Environmental Applications: The compound is being explored for use in sensors and catalysts that can detect and degrade pollutants, contributing to environmental sustainability efforts.

Citations