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Catalog Number:
39634
CAS Number:
247089-85-6
( R )-(-)- p -Toluènesulfinamide
Purity:
≥ 98 % (HPLC)
Synonym(s):
( R )-4-méthylbenzènesulfinamide
Documents
$101.45 /200 mg
Taille
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Informations sur le produit

(R)-(-)-p-Toluenesulfinamide is a valuable chiral sulfinamide compound widely utilized in the synthesis of pharmaceuticals and agrochemicals. This compound is recognized for its ability to act as a versatile building block in asymmetric synthesis, enabling the production of enantiomerically pure compounds that are crucial in drug development. Its unique sulfinamide functional group enhances reactivity and selectivity, making it an essential reagent in various chemical transformations. Researchers and industry professionals benefit from its application in the synthesis of biologically active molecules, including potential therapeutic agents and crop protection products.

Additionally, (R)-(-)-p-Toluenesulfinamide is known for its stability and ease of handling, which are significant advantages over similar compounds. Its use in the pharmaceutical industry has led to the development of novel drugs with improved efficacy and reduced side effects. With its growing relevance in synthetic organic chemistry, this compound is an excellent choice for laboratories focused on innovative research and development.

Numéro CAS 
247089-85-6
Formule moléculaire
C 7 H 9 NOS
Poids moléculaire 
155.22
Point de fusion 
116 - 120 °C
Rotation optique 
[α] 20 D = -91 à -81 ° (C=1 dans CHCl 3 )
Informations générales
Numéro CAS 
247089-85-6
Formule moléculaire
C 7 H 9 NOS
Poids moléculaire 
155.22
Point de fusion 
116 - 120 °C
Rotation optique 
[α] 20 D = -91 à -81 ° (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

(R)-(-)-p-Toluenesulfinamide is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a chiral auxiliary in the synthesis of pharmaceuticals, enabling the production of enantiomerically pure compounds, which is crucial in drug development.
  • Organocatalysis: It acts as an effective organocatalyst in various reactions, enhancing reaction rates and selectivity, which is beneficial in green chemistry practices.
  • Drug Discovery: Researchers leverage its properties to create novel compounds with potential therapeutic effects, particularly in the fields of oncology and neurology.
  • Analytical Chemistry: It is used in the development of analytical methods for the detection and quantification of other compounds, improving accuracy in chemical analysis.
  • Material Science: The compound is explored for its potential in developing new materials with specific electronic or optical properties, which can lead to advancements in technology.

Citations