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Catalog Number:
40964
CAS Number:
131457-46-0
( S , S )-2,2'-isopropylidènebis(4-phényl-2-oxazoline)
Purity:
≥ 97% (CG)
Synonym(s):
( S , S )-2,2-Bis(4-phényl-2-oxazolin-2-yl)propane, ( S , S )-2,2'-(diméthylméthylène)bis(4-phényl-2-oxazoline)
Documents
$111.17 /250 mg
Taille
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Informations sur le produit

(S,S)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline) is a versatile compound known for its unique chiral properties, making it an essential tool in asymmetric synthesis and catalysis. This compound serves as a highly effective ligand in various catalytic processes, particularly in the synthesis of chiral amines and alcohols, which are crucial in the pharmaceutical industry. Its ability to facilitate enantioselective reactions positions it as a valuable resource for researchers and professionals aiming to develop new drugs and fine chemicals with high specificity and efficiency.

Additionally, (S,S)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline) has shown promise in polymer chemistry, where it can be utilized to create advanced materials with tailored properties. Its stability and reactivity make it suitable for applications in the development of functionalized polymers and nanomaterials. The compound's unique structural features allow for fine-tuning of its interactions, enhancing its effectiveness in various applications. With its broad range of uses, this compound is an excellent choice for those looking to innovate in chemical synthesis and material science.

Numéro CAS 
131457-46-0
Formule moléculaire
C21H22N2O2
Poids moléculaire 
334.42
Point de fusion 
37 - 41 °C
Rotation optique 
[α] 20 D = -173 à -151 ° (C = 1 dans EtOH)
Informations générales
Numéro CAS 
131457-46-0
Formule moléculaire
C21H22N2O2
Poids moléculaire 
334.42
Point de fusion 
37 - 41 °C
Rotation optique 
[α] 20 D = -173 à -151 ° (C = 1 dans EtOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

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

  • Chiral Catalysis: This compound serves as an effective chiral ligand in asymmetric catalysis, enhancing the selectivity of reactions in the pharmaceutical industry, which is crucial for developing enantiomerically pure drugs.
  • Polymer Chemistry: It is used in the synthesis of functional polymers, improving material properties such as thermal stability and mechanical strength, which are essential for advanced materials in automotive and aerospace applications.
  • Drug Delivery Systems: The compound can be incorporated into drug delivery formulations, allowing for targeted release and improved bioavailability of therapeutic agents, thereby enhancing treatment efficacy.
  • Biomaterials: Its biocompatibility makes it suitable for use in biomedical applications, such as scaffolds for tissue engineering, promoting cell growth and regeneration in medical implants.
  • Analytical Chemistry: It is employed as a chiral selector in chromatography, facilitating the separation and analysis of complex mixtures, which is vital for quality control in pharmaceutical manufacturing.

Citations