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Catalog Number:
41424
CAS Number:
32587-64-7
S -2,2'-diméthyl-1,1'-binaphtyle
Purity:
≥ 98 % (HPLC)
Documents
$365.05 /1G
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Informations sur le produit

(S)-2,2'-Dimethyl-1,1'-binaphthyl is a versatile chiral compound widely recognized for its applications in asymmetric synthesis and catalysis. This compound, often referred to as DM-BINAP, serves as an essential ligand in various catalytic reactions, particularly in the field of organic chemistry. Its unique structure allows for enhanced selectivity and efficiency in reactions, making it invaluable for researchers aiming to develop new synthetic pathways. The compound's ability to facilitate enantioselective transformations has made it a preferred choice in the pharmaceutical industry, where the production of chiral drugs is critical.

In addition to its role in catalysis, (S)-2,2'-Dimethyl-1,1'-binaphthyl is also utilized in the development of advanced materials and sensors due to its optical properties. Researchers have leveraged its chiral nature to create innovative applications in liquid crystals and optoelectronic devices. With its proven track record in enhancing reaction outcomes and its potential in material science, this compound stands out as a key player in both academic and industrial settings, offering significant advantages over non-chiral alternatives.

Numéro CAS 
32587-64-7
Formule moléculaire
C 22 H 18
Poids moléculaire 
282.39
Rotation optique 
[α] 20 D = 15 - 20° (C = 0,5 en EH (95%))
Informations générales
Numéro CAS 
32587-64-7
Formule moléculaire
C 22 H 18
Poids moléculaire 
282.39
Rotation optique 
[α] 20 D = 15 - 20° (C = 0,5 en EH (95%))
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)-2,2'-Dimethyl-1,1'-binaphthyl is widely utilized in research focused on:

  • Chiral Catalysis: This compound serves as a chiral ligand in asymmetric synthesis, enhancing the efficiency of reactions that produce enantiomerically pure compounds, which is crucial in pharmaceuticals.
  • Organic Electronics: It is used in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics, contributing to advancements in energy-efficient display technologies and solar cells.
  • Material Science: The compound plays a role in creating advanced materials with unique optical and electronic properties, beneficial for applications in sensors and nanotechnology.
  • Research in Stereochemistry: As a model compound, it aids researchers in studying stereochemical properties and behaviors, which is essential for understanding molecular interactions.
  • Drug Development: Its application in drug design helps in the creation of new therapeutic agents, particularly in targeting specific biological pathways with improved efficacy and reduced side effects.

Citations