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Catalog Number:
39492
CAS Number:
126456-43-7
(1 S , 2 R )-(-)-1-Amino-2-indanol
Purity:
≥ 98% (ensayo por titulación, GC)
Synonym(s):
(1 S ,2 R )-(-)-1-Amino-2-hidroxiindano
Documents
$46.77 /1G
Tamaño
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Información del producto

(1S,2R)-(-)-1-Amino-2-indanol is a versatile compound with significant applications in the fields of pharmaceuticals and organic synthesis. This chiral amine is recognized for its role as a building block in the synthesis of various bioactive molecules, particularly in the development of pharmaceuticals targeting neurological disorders. Its unique stereochemistry allows for the creation of enantiomerically pure compounds, which is crucial in drug development to ensure efficacy and minimize side effects.

In addition to its pharmaceutical applications, (1S,2R)-(-)-1-Amino-2-indanol is also utilized in the synthesis of advanced materials and agrochemicals. Researchers appreciate its ability to facilitate complex reactions, making it a valuable asset in laboratories focused on innovative chemical synthesis. With its favorable properties and broad applicability, this compound stands out as an essential tool for professionals seeking to enhance their research and development efforts.

Número CAS
126456-43-7
Fórmula molecular
C 9 H 11 NO
Peso molecular
149.19
Número MDL
MFCD00216655
Punto de fusión
117 °C
Rotación óptica
[α]20 D = -41 a -45 ° (C=1 en MeOH)
Condiciones
Tienda en RT
Información general
Número CAS
126456-43-7
Fórmula molecular
C 9 H 11 NO
Peso molecular
149.19
Número MDL
MFCD00216655
Punto de fusión
117 °C
Rotación óptica
[α]20 D = -41 a -45 ° (C=1 en MeOH)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(1S,2R)-(-)-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 an excellent candidate for asymmetric synthesis, allowing researchers to create enantiomerically pure compounds more efficiently than with other catalysts.
  • Biochemical Research: The compound is used in studies related to enzyme inhibition, providing insights into metabolic pathways and potential therapeutic targets.
  • Material Science: It is explored for its potential in creating novel materials with specific optical or electronic properties, beneficial for the development of advanced devices.
  • Natural Product Synthesis: The compound is applied in the synthesis of complex natural products, aiding researchers in the exploration of bioactive compounds found in nature.

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