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Catalog Number:
41422
CAS Number:
137848-28-3
R -(+)-2-Amino-2'-hydroxy-1,1'-binaphtyle
Purity:
≥ 98 % (pureté chirale)
Synonym(s):
( R -(+)-1-(2-amino-1-naphtyl)-2-naphtol, ( R -(+)-NOBINE, ( R -(+)-2'-Amino-1,1'-binaphtalène-2-ol
Hazmat
Documents
$260.69 /100 mg
Taille
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Informations sur le produit

(R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl is a versatile chiral compound widely recognized for its applications in asymmetric synthesis and catalysis. This compound, often referred to as BINOL derivative, serves as a crucial building block in the development of chiral ligands and catalysts, making it invaluable in the pharmaceutical and fine chemical industries. Its unique structural features allow for enhanced selectivity in reactions, which is essential for producing enantiomerically pure compounds. Researchers and industry professionals utilize this compound in various applications, including the synthesis of complex organic molecules and the development of new drugs, where precision and efficiency are paramount.

The compound's ability to facilitate enantioselective transformations positions it as a preferred choice for chemists looking to optimize reaction conditions and improve yields. Its stability and compatibility with a range of reaction conditions further enhance its appeal, making it a reliable option for both academic research and industrial applications. With its proven track record in catalysis, (R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl stands out as a key player in advancing modern synthetic methodologies.

Numéro CAS 
137848-28-3
Formule moléculaire
C 20 H 15 NON
Poids moléculaire 
0
Point de fusion 
173 °C (lit.)
Rotation optique 
[α] 20 D = 120 ° (C = 1 dans THF)
Informations générales
Numéro CAS 
137848-28-3
Formule moléculaire
C 20 H 15 NON
Poids moléculaire 
0
Point de fusion 
173 °C (lit.)
Rotation optique 
[α] 20 D = 120 ° (C = 1 dans THF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl is widely utilized in research focused on

  • Asymmetric Synthesis: This compound serves as a chiral ligand in asymmetric synthesis, helping researchers create enantiomerically pure compounds, which are crucial in pharmaceuticals.
  • Catalysis: It is employed in catalytic processes, particularly in the synthesis of complex organic molecules, providing high selectivity and efficiency compared to traditional catalysts.
  • Pharmaceutical Development: The compound plays a vital role in drug discovery, particularly in the development of new medications that require specific stereochemistry for efficacy.
  • Material Science: It is used in the creation of advanced materials, such as liquid crystals, due to its unique structural properties, enhancing the performance of electronic devices.
  • Research in Chiral Chemistry: This chemical is a key component in studies exploring chiral resolution techniques, aiding in the understanding of chirality's impact on biological activity.

Citations