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Catalog Number:
41358
CAS Number:
62173-99-3
Benzyl ( S )-(+)-mandélate
Purity:
≥ 98,5 % (CG)
Synonym(s):
L-(+)-mandélate de benzyle, Ester benzylique de l'acide L-(+)-mandélique
Documents
$61.19 /5G
Taille
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Informations sur le produit

Benzyl (S)-(+)-mandelate is a versatile compound widely recognized for its applications in organic synthesis and pharmaceutical development. This chiral mandelate ester is particularly valued for its ability to serve as a chiral auxiliary in asymmetric synthesis, facilitating the production of enantiomerically pure compounds. Its unique structure allows for selective reactions, making it an essential tool for researchers aiming to develop new drugs and fine chemicals. Additionally, Benzyl (S)-(+)-mandelate is utilized in the synthesis of various biologically active molecules, showcasing its relevance in medicinal chemistry.

The compound's favorable properties, including its stability and ease of handling, further enhance its appeal to industry professionals. Its applications extend to the production of flavor and fragrance compounds, where it contributes to the development of novel aromatic profiles. Researchers and manufacturers alike can benefit from the efficiency and effectiveness of Benzyl (S)-(+)-mandelate in their processes, making it a valuable addition to any laboratory or production facility focused on innovation and quality.

Numéro CAS 
62173-99-3
Formule moléculaire
C15H14O3
Poids moléculaire 
242.27
Point de fusion 
104 - 107 °C (lit.)
Rotation optique 
[α] 20 D = 56 ± 3 ° (C = 1 dans CHCl 3 )
Informations générales
Numéro CAS 
62173-99-3
Formule moléculaire
C15H14O3
Poids moléculaire 
242.27
Point de fusion 
104 - 107 °C (lit.)
Rotation optique 
[α] 20 D = 56 ± 3 ° (C = 1 dans CHCl 3 )
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

Benzyl (S)-(+)-mandelate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a chiral building block in the synthesis of various pharmaceuticals, enhancing the efficacy and specificity of drug formulations.
  • Flavor and Fragrance Industry: It is used as a flavoring agent and fragrance component, providing a pleasant aroma and taste in food products and cosmetics.
  • Chiral Resolution: The compound plays a crucial role in the resolution of racemic mixtures, allowing chemists to isolate and utilize the desired enantiomer in various applications.
  • Research in Organic Chemistry: It is a valuable reagent in organic synthesis, facilitating reactions that lead to the formation of complex molecules, which are essential in academic and industrial research.
  • Biochemical Studies: This compound is employed in studies related to enzyme activity and metabolic pathways, helping researchers understand biological processes and develop new therapeutic strategies.

Citations