Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
39500
CAS Number:
163061-73-2
(1 R ,2 R )-(-)-1-Amino-2-indanol
Purity:
≥ 98 % (dosage par titration, pureté chirale, GC)
Synonym(s):
(1 R ,2 R )-(-)-1-amino-2-hydroxyindane
Documents
$55.48 /1G
Taille
Request Bulk Quote
Informations sur le produit

(1R,2R)-(-)-1-Amino-2-indanol is a versatile compound with significant applications in the pharmaceutical and chemical research sectors. This chiral amino alcohol is recognized for its role as a building block in the synthesis of various biologically active molecules, particularly in the development of pharmaceuticals targeting neurological disorders. Its unique stereochemistry allows for specific interactions in biological systems, making it a valuable tool for researchers focused on drug design and development.

Additionally, (1R,2R)-(-)-1-Amino-2-indanol serves as an important intermediate in the synthesis of indole derivatives, which are widely used in medicinal chemistry. Its ability to facilitate the formation of complex molecular structures enhances its utility in creating innovative therapeutic agents. With its favorable properties, this compound stands out for its potential to streamline synthetic pathways and improve yields in laboratory settings, making it an essential addition to any researcher's toolkit.

Numéro CAS 
163061-73-2
Formule moléculaire
C 9 H 11 NON
Poids moléculaire 
149.19
Point de fusion 
144 °C
Rotation optique 
[α]20 D = -24 ° (C=1 dans MeOH)
Informations générales
Numéro CAS 
163061-73-2
Formule moléculaire
C 9 H 11 NON
Poids moléculaire 
149.19
Point de fusion 
144 °C
Rotation optique 
[α]20 D = -24 ° (C=1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

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

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Catalysis: Its unique chiral properties make it valuable in asymmetric synthesis, allowing chemists to create enantiomerically pure compounds, which are essential in drug formulation.
  • Biochemical Research: Researchers use it to study enzyme interactions and protein folding, helping to understand biological processes and disease mechanisms.
  • Material Science: The compound is explored for its potential in creating innovative materials with specific optical or electronic properties, beneficial for developing advanced technologies.
  • Analytical Chemistry: It is employed as a standard in various analytical techniques, aiding in the accurate quantification and characterization of related compounds in complex mixtures.

Citations