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Catalog Number:
41073
CAS Number:
850661-66-4
( S )-4-isopropyl-3-(1-naphtylméthyl)-2,5,5-triphényl-1,3,2-oxazaborolidine (environ 6 % dans le toluène, environ 0,1 mol/L)
Purity:
≥ 98%
Documents
$363.84 /10ML
Taille
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Informations sur le produit

(S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine is a specialized compound known for its unique boron-containing structure, which enhances its reactivity and selectivity in various chemical reactions. This compound is particularly valuable in asymmetric synthesis, where it serves as a chiral catalyst, facilitating the production of enantiomerically pure compounds. Its ability to stabilize transition states makes it an excellent choice for researchers and industry professionals looking to optimize reaction conditions in organic synthesis.

In addition to its role in catalysis, this compound has shown promise in medicinal chemistry, particularly in the development of pharmaceuticals that require precise stereochemistry. Its compatibility with various solvents, such as toluene, allows for flexibility in experimental setups, making it a preferred choice in laboratories focused on innovative chemical research. With its unique properties and practical applications, (S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine stands out as a valuable tool for advancing synthetic methodologies and enhancing the efficiency of chemical processes.

Numéro CAS 
850661-66-4
Formule moléculaire
C 34 H 32 BNO
Poids moléculaire 
481.45
Indice de réfraction 
n20D 1,50
Informations générales
Numéro CAS 
850661-66-4
Formule moléculaire
C 34 H 32 BNO
Poids moléculaire 
481.45
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

(S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a chiral catalyst in asymmetric synthesis, enabling the production of enantiomerically pure compounds, which is crucial in pharmaceuticals for developing effective drugs with fewer side effects.
  • Organocatalysis: It is employed in organocatalytic reactions, providing a more environmentally friendly alternative to traditional metal catalysts, thus reducing toxic waste in chemical processes.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanocomposites, enhancing their properties like strength and thermal stability for applications in electronics and packaging.
  • Drug Development: Its role in drug discovery includes facilitating the synthesis of complex organic molecules, which can lead to new therapeutic agents, particularly in cancer and infectious diseases.
  • Research in Green Chemistry: This chemical contributes to green chemistry initiatives by enabling reactions that minimize energy consumption and reduce hazardous byproducts, aligning with sustainable practices in chemical manufacturing.

Citations