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Catalog Number:
24542
CAS Number:
62961-64-2
-)-D-tartrate de diisopropyle
Purity:
≥ 99% (GC)
Synonym(s):
Ester diisopropylique de l'acide D-(-)-tartrique, (2S,3S)-dihydroxysuccinate de diisopropyle
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Informations sur le produit

(-)-Diisopropyl D-tartrate is a versatile chiral building block widely utilized in organic synthesis and pharmaceutical applications. This compound, known for its high optical purity, serves as an essential reagent in asymmetric synthesis, enabling the production of enantiomerically enriched compounds. Its unique properties make it particularly valuable in the development of chiral catalysts and ligands, which are crucial in the synthesis of various pharmaceuticals and agrochemicals. Researchers and industry professionals appreciate its role in enhancing reaction selectivity and efficiency, ultimately leading to more sustainable and cost-effective processes.

In addition to its applications in synthesis, (-)-Diisopropyl D-tartrate is also employed in the production of various fine chemicals and intermediates. Its ability to facilitate the formation of complex molecular architectures makes it a preferred choice for chemists aiming to innovate in drug discovery and development. With its proven track record in enhancing reaction outcomes and its relevance in cutting-edge research, this compound stands out as a key player in the toolkit of modern synthetic chemists.

Numéro CAS 
62961-64-2
Formule moléculaire
C10H18O6
Poids moléculaire 
234.25
Rotation optique 
-17º ± 1º
Informations générales
Numéro CAS 
62961-64-2
Formule moléculaire
C10H18O6
Poids moléculaire 
234.25
Rotation optique 
-17º ± 1º
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(-)-Diisopropyl D-tartrate is widely utilized in research focused on

  • Chiral Resolution: This compound is commonly used in the pharmaceutical industry for the resolution of racemic mixtures, allowing researchers to isolate and produce specific enantiomers that are often more effective as drugs.
  • Asymmetric Synthesis: It serves as a chiral auxiliary in asymmetric synthesis, enabling chemists to create compounds with a desired stereochemistry, which is crucial in the development of new pharmaceuticals.
  • Biocatalysis: In biochemistry, it is employed as a substrate for enzyme-catalyzed reactions, facilitating the production of chiral compounds in a more environmentally friendly manner.
  • Analytical Chemistry: The compound is utilized in various analytical techniques, such as chromatography, to help differentiate between enantiomers, aiding in quality control and research applications.
  • Food and Beverage Industry: It finds applications in the food industry as a chiral agent to enhance flavors and aromas, contributing to the development of more refined products.

Citations