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Catalog Number:
39644
CAS Number:
184346-45-0
(4 S )-(-)-4-isopropyl-5,5-diphényl-2-oxazolidinone
Purity:
≥ 99 % (pureté chirale)
Synonym(s):
( S )-(-)-4-isopropyl-5,5-diphényl-2-oxazolidinone
Documents
$204.31 /1G
Taille
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Informations sur le produit

(4S)-(-)-4-Isopropyl-5,5-diphenyl-2-oxazolidinone is a versatile compound widely recognized for its applications in pharmaceutical research and development. This chiral oxazolidinone derivative is particularly valuable in the synthesis of various biologically active molecules, serving as a key intermediate in the production of chiral pharmaceuticals. Its unique structure allows for the selective formation of enantiomers, making it an essential tool for chemists aiming to enhance the efficacy and safety profiles of drug candidates.

Moreover, this compound has shown promise in the field of asymmetric synthesis, where it aids in the development of novel therapeutic agents with improved pharmacological properties. Researchers appreciate its ability to facilitate complex reactions while maintaining high levels of stereoselectivity. As a result, (4S)-(-)-4-Isopropyl-5,5-diphenyl-2-oxazolidinone stands out as a crucial component in the toolkit of medicinal chemists and pharmaceutical developers, driving innovation in drug discovery and development.

Numéro CAS 
184346-45-0
Formule moléculaire
C 18 H 19 NO 2
Poids moléculaire 
281.36
Point de fusion 
252 - 256 °C
Rotation optique 
[α] 20 D = -249 à -243 ° (C=0,6 dans CH 2 Cl 2 )
Informations générales
Numéro CAS 
184346-45-0
Formule moléculaire
C 18 H 19 NO 2
Poids moléculaire 
281.36
Point de fusion 
252 - 256 °C
Rotation optique 
[α] 20 D = -249 à -243 ° (C=0,6 dans CH 2 Cl 2 )
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

(4S)-(-)-4-Isopropyl-5,5-diphenyl-2-oxazolidinone is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a chiral auxiliary in the synthesis of various pharmaceuticals, enhancing the efficiency of drug development processes.
  • Asymmetric Synthesis: It plays a crucial role in asymmetric synthesis, allowing researchers to create compounds with specific stereochemistry, which is vital in producing effective medications.
  • Material Science: The compound is used in the development of advanced materials, particularly in creating polymers with unique properties, benefiting industries like packaging and automotive.
  • Catalysis: It acts as a catalyst in several chemical reactions, improving reaction rates and yields, which is essential for chemical manufacturing and industrial processes.
  • Research in Organic Chemistry: This chemical is a valuable tool for organic chemists studying reaction mechanisms and developing new synthetic methodologies, contributing to innovation in the field.

Citations