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Catalog Number:
40328
CAS Number:
197223-39-5
Acide 3,5-di- tert -butylphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3,5-di- tert- butylbenzèneboronique
Documents
$124.99 /200 mg
Taille
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Informations sur le produit

3,5-Di-tert-butylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure, featuring two tert-butyl groups, enhances its solubility and stability, allowing for efficient reactions under various conditions. Researchers and industry professionals appreciate its application in the development of pharmaceuticals, agrochemicals, and advanced materials, where it serves as a key building block for complex molecular architectures.

Additionally, 3,5-Di-tert-butylphenylboronic acid has shown promise in the field of sensor technology, particularly in the detection of biomolecules. Its selective binding properties can be harnessed to create sensitive and specific sensors for glucose and other analytes, highlighting its potential in healthcare applications. With its robust performance and adaptability, this compound stands out as a valuable tool for researchers aiming to innovate in synthetic chemistry and biosensing technologies.

Numéro CAS 
197223-39-5
Formule moléculaire
C 14 H 23 BO 2
Poids moléculaire 
234.15
Point de fusion 
182 °C (lit.)
Indice de réfraction 
n20D 1,50
Informations générales
Numéro CAS 
197223-39-5
Formule moléculaire
C 14 H 23 BO 2
Poids moléculaire 
234.15
Point de fusion 
182 °C (lit.)
Indice de réfraction 
n20D 1,50
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

3,5-Di-tert-butylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in the synthesis of complex organic molecules.
  • Pharmaceutical Development: It plays a significant role in the development of boron-containing drugs, which can enhance the efficacy of therapeutic agents by improving their stability and bioavailability.
  • Material Science: The compound is used in the creation of advanced materials, such as polymers and nanocomposites, due to its ability to modify the properties of materials at the molecular level.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for attaching biomolecules to surfaces or other molecules.
  • Analytical Chemistry: This chemical is employed in sensors and assays for detecting glucose and other biomolecules, offering a reliable method for monitoring biological processes.

Citations