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Catalog Number:
41431
CAS Number:
126613-06-7
R -(-)-1,1'-binaphtyl-2,2'-diyl bis(trifluorométhanesulfonate)
Purity:
≥ 96 % (HPLC)
Synonym(s):
( R -(-)-1,1'-Bi-2-naphtol bis(trifluorométhanesulfonate)
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Informations sur le produit

(R)-(-)-1,1'-Binaphthyl-2,2'-diyl bis(trifluoromethanesulfonate) is a highly versatile compound widely utilized in asymmetric synthesis and catalysis. This chiral bis(trifluoromethanesulfonate) derivative is recognized for its ability to facilitate enantioselective reactions, making it an invaluable tool for researchers in the fields of organic chemistry and pharmaceuticals. Its unique trifluoromethanesulfonate groups enhance reactivity and selectivity, allowing for the efficient formation of complex molecular architectures.

In practical applications, this compound has been effectively employed in the synthesis of various biologically active molecules, including pharmaceuticals and agrochemicals. Its ability to promote high yields and selectivity in reactions positions it as a preferred choice for chemists aiming to develop new compounds with specific properties. Additionally, its stability and ease of handling make it suitable for both laboratory and industrial settings, ensuring that researchers can achieve their desired outcomes with confidence.

Numéro CAS 
126613-06-7
Formule moléculaire
C 22 H 12 F 6 O 6 S 2
Poids moléculaire 
0
Point de fusion 
82 - 87 °C
Rotation optique 
[α] 20 D = -154 à -135 ° (C = 1 dans THF)
Informations générales
Numéro CAS 
126613-06-7
Formule moléculaire
C 22 H 12 F 6 O 6 S 2
Poids moléculaire 
0
Point de fusion 
82 - 87 °C
Rotation optique 
[α] 20 D = -154 à -135 ° (C = 1 dans THF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(R)-(-)-1,1'-Binaphthyl-2,2'-diyl bis(trifluoromethanesulfonate) is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a chiral auxiliary in asymmetric synthesis, enabling chemists to create specific enantiomers of molecules, which is crucial in pharmaceuticals where the efficacy of a drug can depend on its chirality.
  • Catalysis: It is used in catalytic reactions, particularly in the production of fine chemicals. Its unique structure allows for enhanced reaction rates and selectivity, making it valuable in industrial applications.
  • Material Science: This chemical is applied in developing advanced materials, such as polymers and coatings, that require specific optical or electronic properties, benefiting industries like electronics and coatings.
  • Research in Organocatalysis: It plays a significant role in organocatalysis, where it helps facilitate reactions without the need for metal catalysts, offering a greener alternative in organic synthesis.
  • Pharmaceutical Development: The compound is explored for its potential in drug formulation, particularly in enhancing the solubility and bioavailability of active pharmaceutical ingredients, addressing common challenges in drug delivery.

Citations