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Catalog Number:
39483
CAS Number:
23364-44-5
(1 S ,2 R )-(+)-2-Amino-1,2-diphényléthanol
Purity:
≥ 99 % (HPLC chirale, HPLC)
Documents
$18.50 /5G
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Informations sur le produit

(1S,2R)-(+)-2-Amino-1,2-diphenylethanol is a versatile chiral amine that plays a significant role in various fields, particularly in pharmaceuticals and organic synthesis. This compound is recognized for its ability to act as a building block in the synthesis of biologically active molecules, making it invaluable for researchers focused on drug development. Its unique chiral properties allow for the creation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry to ensure efficacy and safety in drug formulations.

Additionally, (1S,2R)-(+)-2-Amino-1,2-diphenylethanol is utilized in asymmetric synthesis, where it serves as a catalyst or reagent in reactions that require high selectivity. Its application extends to the production of various fine chemicals and agrochemicals, showcasing its importance in both chemical research and industrial applications. With its reliable performance and ability to enhance reaction outcomes, this compound is an essential resource for professionals seeking to innovate and optimize their chemical processes.

Numéro CAS 
23364-44-5
Formule moléculaire
C 14 H 15 NON
Poids moléculaire 
213.28
Point de fusion 
141 - 144 °C
Rotation optique 
[a] D 20 = 6 - 8 ° (C = 0,6 dans EtOH)
Informations générales
Numéro CAS 
23364-44-5
Formule moléculaire
C 14 H 15 NON
Poids moléculaire 
213.28
Point de fusion 
141 - 144 °C
Rotation optique 
[a] D 20 = 6 - 8 ° (C = 0,6 dans EtOH)
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

(1S,2R)-(+)-2-Amino-1,2-diphenylethanol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a chiral building block in the synthesis of various pharmaceuticals, enhancing the efficacy and safety of drugs by enabling the production of enantiomerically pure compounds.
  • Catalysis: It is employed as a ligand in asymmetric catalysis, facilitating reactions that produce specific stereoisomers, which are crucial in the manufacture of fine chemicals and agrochemicals.
  • Biochemical Research: Researchers use this compound to study its interactions with biological systems, contributing to the understanding of enzyme mechanisms and receptor binding, which is vital in drug discovery.
  • Material Science: The compound's unique properties make it suitable for developing advanced materials, such as polymers and composites, that require specific mechanical and thermal characteristics.
  • Chiral Separation Techniques: It is utilized in chiral chromatography for the separation of enantiomers, which is essential in various industries, including food and beverage, to ensure product quality and regulatory compliance.

Citations