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Catalog Number:
39499
CAS Number:
163061-74-3
(1 S ,2 S )-(+)-1-Amino-2-indanol
Purity:
≥ 98 % (pureté chirale, GC)
Synonym(s):
(1 S ,2 S )-(+)-1-Amino-2-hydroxyindane
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Informations sur le produit

(1S,2S)-(+)-1-Amino-2-indanol is a versatile compound recognized for its unique structural properties and potential applications in various fields. This chiral amino alcohol is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral intermediates for drug formulations. Its ability to act as a building block in asymmetric synthesis makes it invaluable for researchers focusing on drug discovery and development. Additionally, its properties allow for the creation of novel compounds that can exhibit enhanced biological activity, making it a key player in medicinal chemistry.

Moreover, (1S,2S)-(+)-1-Amino-2-indanol has shown promise in the field of organic synthesis, where it can be employed in the preparation of complex molecules. Its unique stereochemistry provides an advantage in producing enantiomerically pure substances, which are crucial for the efficacy and safety of pharmaceutical products. Researchers and industry professionals can leverage this compound to streamline their synthesis processes, reduce waste, and improve yields, ultimately leading to more efficient and effective drug development.

Numéro CAS 
163061-74-3
Formule moléculaire
C 9 H 11 NON
Poids moléculaire 
149.19
Point de fusion 
146 °C
Rotation optique 
[α]20 D = 24 ° (C=1 dans MeOH)
Informations générales
Numéro CAS 
163061-74-3
Formule moléculaire
C 9 H 11 NON
Poids moléculaire 
149.19
Point de fusion 
146 °C
Rotation optique 
[α]20 D = 24 ° (C=1 dans MeOH)
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 
-
Applications

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

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Catalysis: Its chiral properties make it valuable in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds more efficiently than with non-chiral catalysts.
  • Biochemical Research: Researchers use this compound to study its effects on neurotransmitter systems, contributing to the understanding of mood disorders and potential treatments.
  • Material Science: It can be incorporated into polymer formulations, enhancing the mechanical properties and thermal stability of materials used in various applications.
  • Analytical Chemistry: The compound is utilized as a standard in chromatographic techniques, aiding in the accurate analysis of related compounds in complex mixtures.

Citations