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Catalog Number:
41056
CAS Number:
111795-43-8
( R )-3,3'-Dibromo-1,1'-bi-2-naphtol
Purity:
≥ 98 % (pureté chirale)
Synonym(s):
( R )-3,3'-dibromo-2,2'-dihydroxy-1,1'-binaphtyle
Documents
$380.57 /1G
Taille
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Informations sur le produit

(R)-3,3'-Dibromo-1,1'-bi-2-naphthol is a specialized compound known for its unique properties and applications in various fields, particularly in organic synthesis and materials science. This compound features two bromine atoms and hydroxyl groups that enhance its reactivity, making it an excellent candidate for use in asymmetric synthesis and catalysis. Its chirality allows for the production of enantiomerically pure compounds, which is crucial in pharmaceutical applications where the efficacy of drugs can depend on their stereochemistry.

In addition to its role in synthesis, (R)-3,3'-Dibromo-1,1'-bi-2-naphthol is also utilized in the development of advanced materials, such as organic light-emitting diodes (OLEDs) and liquid crystal displays (LCDs). Its ability to act as a ligand in coordination chemistry further expands its utility in creating novel compounds with tailored properties. Researchers and industry professionals can leverage this compound for innovative applications, making it a valuable addition to any chemical inventory.

Numéro CAS 
111795-43-8
Formule moléculaire
C20H12Br2O2
Poids moléculaire 
444.12
Point de fusion 
256 - 260 °C
Rotation optique 
[α] 20 D = 90 ± 2 ° (C = 1 dans MeOH)
Informations générales
Numéro CAS 
111795-43-8
Formule moléculaire
C20H12Br2O2
Poids moléculaire 
444.12
Point de fusion 
256 - 260 °C
Rotation optique 
[α] 20 D = 90 ± 2 ° (C = 1 dans MeOH)
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

(R)-3,3'-Dibromo-1,1'-bi-2-naphthol is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, allowing researchers to create complex molecules with specific properties, enhancing the efficiency of synthetic pathways.
  • Chiral Catalysis: Its unique chiral structure makes it an excellent catalyst in asymmetric synthesis, helping to produce enantiomerically pure compounds, which is crucial in pharmaceuticals.
  • Material Science: Used in the development of advanced materials, it contributes to the creation of polymers and coatings with improved thermal and mechanical properties, benefiting industries like electronics and automotive.
  • Biological Research: This compound is explored for its potential applications in medicinal chemistry, particularly in the design of new drugs targeting specific biological pathways, offering innovative solutions for health challenges.
  • Environmental Chemistry: It plays a role in the study of environmental pollutants, aiding researchers in understanding the behavior of brominated compounds in ecosystems and developing strategies for remediation.

Citations