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Catalog Number:
41059
CAS Number:
80655-81-8
( S )-(+)-6,6'-dibromo-1,1'-bi-2-naphtol
Purity:
≥ 98 % (HPLC)
Synonym(s):
( S )-(+)-6,6'-dibromo-2,2'-dihydroxy-1,1'-binaphtyle
Documents
$158.94 /1G
Taille
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Informations sur le produit

(S)-(+)-6,6'-Dibromo-1,1'-bi-2-naphthol is a versatile compound recognized for its unique properties and applications in various fields, particularly in organic synthesis and material science. This compound, also known as 6,6'-dibromo-2,2'-bi-1-naphthol, serves as an important chiral building block in the synthesis of pharmaceuticals and agrochemicals. Its ability to act as a chiral ligand makes it invaluable in asymmetric catalysis, where it can enhance the selectivity and yield of desired products. Researchers have utilized this compound in the development of novel catalysts and in the study of complex reaction mechanisms, showcasing its relevance in advancing chemical research.

In addition to its synthetic applications, (S)-(+)-6,6'-Dibromo-1,1'-bi-2-naphthol is also explored for its potential in the development of advanced materials, including organic light-emitting diodes (OLEDs) and liquid crystal displays (LCDs). Its unique structural features contribute to improved performance characteristics in these applications. With its dual functionality as a chiral agent and a material component, this compound stands out for its versatility and effectiveness, making it a valuable asset for researchers and industry professionals alike.

Numéro CAS 
80655-81-8
Formule moléculaire
C20H12Br2O2
Poids moléculaire 
444.12
Point de fusion 
195 - 199 °C (lit.)
Rotation optique 
[α] 20 D = 43 - 49 ° (C = 2 dans THF)
Informations générales
Numéro CAS 
80655-81-8
Formule moléculaire
C20H12Br2O2
Poids moléculaire 
444.12
Point de fusion 
195 - 199 °C (lit.)
Rotation optique 
[α] 20 D = 43 - 49 ° (C = 2 dans THF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(S)-(+)-6,6'-Dibromo-1,1'-bi-2-naphthol is widely utilized in research focused on

  • Asymmetric Synthesis: This compound serves as a chiral ligand in asymmetric synthesis, enabling the production of enantiomerically pure compounds, which is crucial in pharmaceuticals.
  • Organic Electronics: It is used in the development of organic light-emitting diodes (OLEDs), enhancing the efficiency and color purity of displays in consumer electronics.
  • Catalysis: The compound acts as a catalyst in various chemical reactions, improving reaction rates and selectivity, which is beneficial in fine chemical manufacturing.
  • Research in Material Science: It is explored for its properties in creating advanced materials, such as polymers with specific optical and electronic characteristics.
  • Biological Studies: The compound is investigated for its potential applications in biological systems, including its role in studying enzyme mechanisms and drug interactions.

Citations