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Catalog Number:
39171
CAS Number:
94594-90-8
(-)-10,2-Camphre sultame
Purity:
≥ 98% (CG)
Synonym(s):
(2 R )-Bornane-10,2-sultame, (-)-exo-10,2-bornanesultame
Documents
$18.53 /1G
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Informations sur le produit

(-)-10,2-Camphorsultam is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This chiral sulfonamide derivative is recognized for its unique structural properties, which enhance its role as a chiral auxiliary in asymmetric synthesis. Its ability to facilitate the formation of enantiomerically enriched compounds makes it invaluable in the development of pharmaceuticals, particularly in the synthesis of biologically active molecules. Researchers appreciate its effectiveness in various reactions, including the formation of amines and the synthesis of complex natural products, where precision and chirality are paramount.

Additionally, (-)-10,2-Camphorsultam exhibits notable stability and compatibility with a range of reaction conditions, making it a reliable choice for both academic and industrial applications. Its distinctive features, such as the presence of a sulfonamide group, contribute to its utility in enhancing reaction selectivity and yield. This compound stands out in the field of asymmetric synthesis, offering significant advantages over other chiral auxiliaries, particularly in terms of ease of use and efficiency in producing high-purity products.

Numéro CAS 
94594-90-8
Formule moléculaire
C 10 H 17 NO 2 S
Poids moléculaire 
215.31
Point de fusion 
182 - 186 °C
Rotation optique 
[α] 20 D = -30 à -32 ° (C = 1 dans CHCl 3 )
Informations générales
Numéro CAS 
94594-90-8
Formule moléculaire
C 10 H 17 NO 2 S
Poids moléculaire 
215.31
Point de fusion 
182 - 186 °C
Rotation optique 
[α] 20 D = -30 à -32 ° (C = 1 dans CHCl 3 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(-)-10,2-Camphorsultam is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a chiral auxiliary in asymmetric synthesis, helping researchers create enantiomerically pure compounds more efficiently.
  • Pharmaceutical Development: It is used in the design of new drugs, particularly in the development of analgesics and anti-inflammatory agents, enhancing the efficacy of medicinal compounds.
  • Material Science: The compound is applied in the formulation of polymers and resins, providing improved thermal stability and mechanical properties compared to traditional materials.
  • Biochemistry: It acts as a reagent in various biochemical assays, aiding in the study of enzyme activities and interactions, which is crucial for drug discovery.
  • Chiral Catalysis: Its unique structure allows it to be used as a catalyst in chiral reactions, offering advantages in selectivity and yield over other catalysts.

Citations