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Catalog Number:
37550
CAS Number:
60646-30-2
S -(+)-2,2,2-Trifluoro-1-(9-anthryl)éthanol [ee Réactif de détermination par RMN]
Purity:
≥ 99% (GC)
Synonym(s):
( S -(+)-1-(9-Anthryl)-2,2,2-trifluoroéthanol, ( S -(+)-α-(trifluorométhyl)-9-anthracénéméthanol
Documents
$98.65 /100 mg
Taille
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Informations sur le produit

(S)-(+)-2,2,2-Trifluoro-1-(9-anthryl)ethanol is a specialized reagent widely utilized in the field of NMR spectroscopy for enantiomeric excess determination. This compound stands out due to its unique trifluoromethyl group, which enhances its solubility and reactivity, making it particularly effective in chiral recognition applications. Researchers in organic chemistry and pharmaceuticals can leverage this compound to analyze the purity and stereochemistry of chiral compounds, thereby facilitating the development of enantiomerically pure drugs. Its ability to provide clear NMR signals allows for accurate and efficient analysis, making it an invaluable tool in both academic and industrial laboratories.

In addition to its analytical applications, (S)-(+)-2,2,2-Trifluoro-1-(9-anthryl)ethanol can also serve as a building block in the synthesis of more complex fluorinated compounds, which are increasingly important in medicinal chemistry. The trifluoromethyl group imparts unique properties that can enhance biological activity, making this compound a promising candidate for further research and development in drug discovery.

Numéro CAS 
60646-30-2
Formule moléculaire
C 16 H 11 F 3 O
Poids moléculaire 
276.26
Point de fusion 
134 - 136 °C
Rotation optique 
[α]20 D = 27 - 34 ° (C=1, CHCl 3 )
Informations générales
Numéro CAS 
60646-30-2
Formule moléculaire
C 16 H 11 F 3 O
Poids moléculaire 
276.26
Point de fusion 
134 - 136 °C
Rotation optique 
[α]20 D = 27 - 34 ° (C=1, 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

(S)-(+)-2,2,2-Trifluoro-1-(9-anthryl)ethanol is widely utilized in research focused on:

  • Chiral Resolution: This compound serves as an effective reagent for determining enantiomeric excess in chiral compounds, which is crucial in pharmaceuticals where the activity can differ significantly between enantiomers.
  • NMR Spectroscopy: It is commonly used in NMR spectroscopy for the analysis of complex mixtures, allowing researchers to identify and quantify specific compounds with high precision.
  • Organic Synthesis: The chemical plays a role in organic synthesis as a building block for creating other fluorinated compounds, which are valuable in various chemical applications.
  • Material Science: Its unique properties make it useful in the development of advanced materials, particularly in the creation of polymers with enhanced thermal and chemical resistance.
  • Pharmaceutical Development: In drug formulation, it aids in optimizing the solubility and stability of active pharmaceutical ingredients, thereby improving drug efficacy and shelf life.

Citations