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Catalog Number:
40987
CAS Number:
150529-93-4
( R , R )-2,2'-isopropylidènebis(4-phényl-2-oxazoline)
Purity:
≥ 98 % (pureté chirale)
Synonym(s):
( R , R )-2,2-Bis(4-phényl-2-oxazolin-2-yl)propane, ( R , R )-2,2'-(diméthylméthylène)bis(4-phényl-2-oxazoline)
Documents
$97.25 /250 mg
Taille
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Informations sur le produit

(R,R)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline) is a versatile compound widely recognized for its applications in the field of asymmetric catalysis and polymer chemistry. This chiral ligand is particularly valued for its ability to facilitate enantioselective reactions, making it an essential tool for researchers aiming to synthesize complex organic molecules with high precision. Its unique structure allows for effective coordination with various metal catalysts, enhancing reaction rates and selectivity.

In addition to its role in catalysis, (R,R)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline) is also utilized in the development of advanced materials, including functional polymers and nanocomposites. Its properties enable the formation of stable complexes that can improve the mechanical and thermal characteristics of polymeric materials. Researchers and industry professionals can leverage this compound to innovate in fields such as drug delivery systems, coatings, and sensors, where enhanced performance and specificity are crucial.

Numéro CAS 
150529-93-4
Formule moléculaire
C21H22N2O2
Poids moléculaire 
334.42
Point de fusion 
56 - 58 °C (lit.)
Rotation optique 
[α] 20 D = 160 ± 2 ° (C = 1 dans EtOH)
Informations générales
Numéro CAS 
150529-93-4
Formule moléculaire
C21H22N2O2
Poids moléculaire 
334.42
Point de fusion 
56 - 58 °C (lit.)
Rotation optique 
[α] 20 D = 160 ± 2 ° (C = 1 dans EtOH)
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

(R,R)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline) is widely utilized in research focused on:

  • Chiral Catalysis: This compound serves as a chiral ligand in asymmetric catalysis, enhancing reaction selectivity and efficiency in the synthesis of pharmaceuticals and fine chemicals.
  • Polymer Chemistry: It is used in the development of novel polymeric materials, providing unique properties such as improved thermal stability and mechanical strength, which are crucial for applications in packaging and automotive industries.
  • Drug Delivery Systems: The compound can be incorporated into drug delivery formulations, improving the solubility and bioavailability of active pharmaceutical ingredients, which is essential for effective therapeutic outcomes.
  • Analytical Chemistry: It is employed as a chiral selector in high-performance liquid chromatography (HPLC), allowing for the separation and analysis of enantiomers in complex mixtures, which is vital for quality control in drug manufacturing.
  • Biomaterials: The compound is explored for use in biocompatible materials, particularly in tissue engineering and regenerative medicine, due to its favorable interactions with biological systems.

Citations