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Catalog Number:
39401
CAS Number:
188447-91-8
( S )-(+)- p -Toluensulfinamida
Purity:
≥ 98 % (HPLC)
Documents
$273.61 /1G
Tamaño
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Información del producto

(S)-(+)-p-Toluenesulfinamide is a versatile chemical compound widely utilized in the synthesis of pharmaceuticals and agrochemicals. This compound, characterized by its sulfinamide functional group, serves as a crucial intermediate in the production of various biologically active molecules. Its unique chiral properties make it particularly valuable in asymmetric synthesis, allowing researchers to create compounds with specific stereochemistry essential for drug efficacy.

In the pharmaceutical industry, (S)-(+)-p-Toluenesulfinamide is employed in the development of chiral drugs, enhancing the effectiveness and safety profiles of therapeutic agents. Additionally, its application extends to the agrochemical sector, where it plays a role in formulating crop protection products. The compound's stability and reactivity under various conditions further bolster its appeal, making it a preferred choice for researchers and industry professionals seeking reliable and efficient building blocks for complex chemical syntheses.

Número CAS
188447-91-8
Fórmula molecular
C7H9NOS
Peso molecular
155.22
Número MDL
MFCD06858375
Punto de fusión
118 - 122 °C
Rotación óptica
[α]20 D = 82 - 87 ° (C=1 en CHCl 3 )
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
188447-91-8
Fórmula molecular
C7H9NOS
Peso molecular
155.22
Número MDL
MFCD06858375
Punto de fusión
118 - 122 °C
Rotación óptica
[α]20 D = 82 - 87 ° (C=1 en CHCl 3 )
Condiciones
Conservar entre 2 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

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

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting neurological disorders.
  • Chiral Catalysis: It is employed in asymmetric synthesis, acting as a chiral auxiliary to produce enantiomerically pure compounds, which is crucial in the production of effective medications.
  • Organic Synthesis: Researchers use it in diverse organic reactions, including the preparation of sulfinamides, which are important in medicinal chemistry for their biological activity.
  • Bioconjugation: The compound is utilized in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Analytical Chemistry: It is also applied in analytical methods for detecting and quantifying amines, providing valuable data in various chemical analyses.

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