Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
30717
CAS Number:
167316-27-0
1 S ,2 S -(+)- N - p -Tosyl-1,2-diphényléthylènediamine
Purity:
≥ 99 % (dosage, pureté chirale)
Documents
$51.18 /1G
Taille
Request Bulk Quote
Informations sur le produit

(1S,2S)-(+)-N-p-Tosyl-1,2-diphenylethylenediamine is a versatile compound widely utilized in asymmetric synthesis and catalysis. This chiral diamine serves as an essential ligand in various catalytic reactions, particularly in the formation of chiral amines and other valuable intermediates. Its unique structure, featuring a tosyl group, enhances its reactivity and selectivity, making it a preferred choice for researchers aiming to develop enantiomerically pure compounds.

In the pharmaceutical industry, this compound plays a crucial role in the synthesis of biologically active molecules, contributing to the development of new drugs and therapeutic agents. Its ability to facilitate enantioselective transformations allows chemists to create compounds with specific desired properties, thereby streamlining the drug discovery process. Additionally, (1S,2S)-(+)-N-p-Tosyl-1,2-diphenylethylenediamine is recognized for its stability and ease of handling, making it an ideal candidate for both academic research and industrial applications.

Numéro CAS 
167316-27-0
Formule moléculaire
C21H22N2O2S
Poids moléculaire 
366.48
Point de fusion 
124-129 °C
Rotation optique 
[a] D 20 = +33° à +36º (C=1 dans CHCl 3 )
Informations générales
Numéro CAS 
167316-27-0
Formule moléculaire
C21H22N2O2S
Poids moléculaire 
366.48
Point de fusion 
124-129 °C
Rotation optique 
[a] D 20 = +33° à +36º (C=1 dans CHCl 3 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(1S,2S)-(+)-N-p-Tosyl-1,2-diphenylethylenediamine is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a chiral auxiliary in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds efficiently, which is crucial in pharmaceuticals.
  • Catalysis: It is employed in catalytic processes, particularly in the synthesis of complex organic molecules, enhancing reaction selectivity and yield compared to traditional catalysts.
  • Drug Development: Researchers use this compound in the development of new drugs, especially in creating compounds that target specific biological pathways, improving therapeutic efficacy.
  • Material Science: It finds applications in the development of advanced materials, such as polymers and nanomaterials, due to its unique structural properties that enhance material performance.
  • Analytical Chemistry: This chemical is utilized in various analytical techniques, including chromatography and spectroscopy, to improve the separation and identification of complex mixtures.

Citations