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Catalog Number:
39642
CAS Number:
188447-91-8
( S )-(+)- p -Toluènesulfinamide
Purity:
≥ 98 % (HPLC)
Documents
$273.61 /1G
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Informations sur le produit

(S)-(+)-p-Toluenesulfinamide is a versatile compound widely utilized in the synthesis of pharmaceuticals and agrochemicals. This chiral sulfinamide is recognized for its ability to act as a chiral auxiliary, facilitating asymmetric synthesis in various chemical reactions. Its unique structure allows for the selective formation of enantiomers, making it invaluable in the development of enantiopure compounds, which are crucial in the pharmaceutical industry for enhancing drug efficacy and reducing side effects.

In addition to its applications in drug synthesis, (S)-(+)-p-Toluenesulfinamide is also employed in the preparation of biologically active compounds and can serve as a key intermediate in the production of sulfonamides. Researchers appreciate its stability and ease of use, which streamline the synthesis process. With its growing importance in medicinal chemistry and its potential to improve the efficiency of chemical reactions, (S)-(+)-p-Toluenesulfinamide stands out as a significant tool for chemists and industry professionals alike.

Numéro CAS 
188447-91-8
Formule moléculaire
C 7 H 9 NOS
Poids moléculaire 
155.22
Point de fusion 
118 - 122 °C
Rotation optique 
[α] 20 D = 82 - 87 ° (C=1 dans CHCL 3 )
Informations générales
Numéro CAS 
188447-91-8
Formule moléculaire
C 7 H 9 NOS
Poids moléculaire 
155.22
Point de fusion 
118 - 122 °C
Rotation optique 
[α] 20 D = 82 - 87 ° (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

(S)-(+)-p-Toluenesulfinamide is widely utilized in research focused on

  • Synthesis of Pharmaceuticals: This compound is a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of chiral drugs, which are essential for enhancing therapeutic efficacy.
  • Asymmetric Catalysis: It serves as an effective chiral auxiliary in asymmetric synthesis, allowing researchers to produce compounds with specific stereochemistry, which is crucial in drug development.
  • Organic Synthesis: The compound is employed in organic reactions, such as the preparation of sulfinamides, which are valuable in creating diverse chemical entities used in agrochemicals and fine chemicals.
  • Research in Material Science: It finds applications in the development of new materials, particularly in creating polymers with enhanced properties, benefiting industries like electronics and coatings.
  • Biochemical Studies: This sulfinamide is used in biochemical research to study enzyme mechanisms and interactions, providing insights that can lead to the discovery of new therapeutic targets.

Citations