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Catalog Number:
39399
CAS Number:
184346-45-0
(4 S )-(-)-4-isopropyl-5,5-diphényl-2-oxazolidinone
Purity:
≥ 99 % (pureté chirale)
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 known for its unique chiral properties, making it an essential building block in the synthesis of pharmaceuticals and agrochemicals. This oxazolidinone derivative is particularly valued in asymmetric synthesis, where its chiral center can facilitate the production of enantiomerically pure compounds. Researchers and industry professionals utilize this compound in the development of novel drugs, especially in the fields of anti-infectives and anti-cancer agents, due to its ability to enhance biological activity and selectivity.

Additionally, (4S)-(-)-4-Isopropyl-5,5-diphenyl-2-oxazolidinone serves as a valuable ligand in catalysis, promoting efficient reactions in various organic transformations. Its stability and compatibility with a wide range of reaction conditions make it a preferred choice for chemists looking to optimize their synthetic pathways. With its proven track record in enhancing the efficacy of active pharmaceutical ingredients, this compound stands out as a crucial asset in modern chemical research 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 = -243 à -249 ° (C=0,6 dans CH2Cl2)
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 = -243 à -249 ° (C=0,6 dans CH2Cl2)
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

(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 and selectivity of drug production.
  • Asymmetric Synthesis: It plays a crucial role in asymmetric synthesis, allowing chemists to create compounds with specific stereochemistry, which is vital for the effectiveness of many drugs.
  • Research in Organic Chemistry: Used extensively in organic synthesis, it aids researchers in developing new methodologies for creating complex organic molecules.
  • Material Science: The compound can be used in the development of novel materials with specific properties, such as polymers that require precise molecular arrangements.
  • Biochemical Applications: It has potential applications in biochemistry, particularly in studying enzyme mechanisms and interactions due to its ability to form stable complexes.

Citations