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Catalog Number:
40327
CAS Number:
149507-36-8
Acide 4-méthoxy-3-(trifluorométhyl)phénylboronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 4-méthoxy-3-(trifluorométhyl)benzèneboronique
Documents
$62.59 /200 mg
Taille
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Informations sur le produit

4-Methoxy-3-(trifluoromethyl)phenylboronic acid is a versatile boronic acid derivative known for its unique trifluoromethyl group, which enhances its reactivity and selectivity in various chemical reactions. This compound is particularly valuable in the field of organic synthesis, where it serves as a key building block for the development of pharmaceuticals and agrochemicals. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it an essential reagent for creating complex molecules with precision. Researchers and industry professionals can leverage its properties to synthesize biologically active compounds, contributing to advancements in drug discovery and development.

Additionally, 4-Methoxy-3-(trifluoromethyl)phenylboronic acid exhibits excellent solubility in organic solvents, facilitating its use in diverse reaction conditions. Its trifluoromethyl group not only improves the electronic properties of the compound but also enhances the stability of the resulting products. This makes it a preferred choice for chemists looking to optimize reaction yields and selectivity. With its broad applicability and unique features, this boronic acid derivative stands out as a valuable tool in modern synthetic chemistry.

Numéro CAS 
149507-36-8
Formule moléculaire
C8H8BF3O3
Poids moléculaire 
219.95
Point de fusion 
202 °C (lit.)
Informations générales
Numéro CAS 
149507-36-8
Formule moléculaire
C8H8BF3O3
Poids moléculaire 
219.95
Point de fusion 
202 °C (lit.)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

4-Methoxy-3-(trifluoromethyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs and crop protection agents.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry, making it invaluable for researchers in synthetic chemistry.
  • Fluorinated Compounds: The trifluoromethyl group enhances the bioactivity of compounds. This property is particularly beneficial in medicinal chemistry, where increased potency and selectivity are desired.
  • Analytical Chemistry: This chemical can be employed in the development of sensors and probes due to its unique reactivity, aiding in the detection of various analytes in environmental and biological samples.
  • Material Science: It is used in the modification of polymers and materials, improving their properties for applications in electronics and coatings, thus enhancing performance and durability.

Citations