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Catalog Number:
40254
CAS Number:
85199-06-0
Acide 2,5-diméthylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2,5-diméthylbenzèneboronique, Acide p-xylène-2-boronique
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$30.85 /1G
Taille
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Informations sur le produit

2,5-Dimethylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for selective functionalization, which is crucial in the development of pharmaceuticals and agrochemicals. Researchers have effectively employed 2,5-Dimethylphenylboronic acid in the synthesis of various biologically active compounds, showcasing its potential in drug discovery and development.

In addition to its role in organic synthesis, 2,5-Dimethylphenylboronic acid is also recognized for its applications in sensor technology and materials science. Its ability to interact with carbohydrates and other biomolecules opens avenues for the development of biosensors and diagnostic tools. The compound's stability and reactivity make it an attractive choice for researchers looking to innovate in these fields. With its broad range of applications and benefits, 2,5-Dimethylphenylboronic acid stands out as a valuable tool for professionals in chemistry and related industries.

Numéro CAS 
85199-06-0
Formule moléculaire
C 8 H 11 BO 2
Poids moléculaire 
149.98
Point de fusion 
192 °C (lit.)
Informations générales
Numéro CAS 
85199-06-0
Formule moléculaire
C 8 H 11 BO 2
Poids moléculaire 
149.98
Point de fusion 
192 °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

2,5-Dimethylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, enhancing the efficiency of chemical reactions.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds, making it valuable in the production of fine chemicals.
  • Sensor Development: The compound is used in the fabrication of sensors for detecting biomolecules, offering high sensitivity and selectivity, which is beneficial in medical diagnostics and environmental monitoring.
  • Material Science: It contributes to the development of advanced materials, including polymers and nanomaterials, which are used in electronics and coatings, providing improved performance and durability.
  • Biological Applications: This boronic acid derivative is explored for its potential in drug delivery systems and as a therapeutic agent, particularly in targeting specific biological pathways, thus presenting a promising avenue in medicinal chemistry.

Citations