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Catalog Number:
37517
CAS Number:
82398-30-9
( R , R -(+)-Clorhidrato de bis(α-metilbencil)amina
Purity:
≥ 98 % (T) (HPLC)
Synonym(s):
Clorhidrato de (+)-Bis[( R -1-feniletil]amina, Clorhidrato de [ R -( R , R )]-(+)-Bis(α-metilbencil)amina
Documents
$441.26 /5G
Tamaño
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Información del producto

(R,R)-(+)-Bis(a-methylbenzyl)amine hydrochloride is a versatile chiral amine that plays a significant role in asymmetric synthesis and pharmaceutical applications. This compound is recognized for its ability to act as a chiral auxiliary, facilitating the production of enantiomerically pure compounds, which is crucial in the development of various pharmaceuticals. Its unique structure allows for enhanced selectivity in reactions, making it an invaluable tool for researchers in the fields of medicinal chemistry and drug development.

In addition to its synthetic utility, (R,R)-(+)-Bis(a-methylbenzyl)amine hydrochloride is also employed in the production of agrochemicals and fine chemicals, where its chiral properties can lead to improved efficacy and reduced side effects. Its stability and ease of handling further enhance its appeal for industrial applications. With its broad range of uses, this compound is essential for professionals seeking to innovate in the synthesis of complex molecules while ensuring high purity and efficiency.

Número CAS
82398-30-9
Fórmula molecular
C16H19N · HCl
Peso molecular
261.79
Número MDL
MFCD00216672
Rotación óptica
[α]20 D = 70 - 76 ° (C=3, EtOH)
Condiciones
Tienda en RT
Información general
Número CAS
82398-30-9
Fórmula molecular
C16H19N · HCl
Peso molecular
261.79
Número MDL
MFCD00216672
Rotación óptica
[α]20 D = 70 - 76 ° (C=3, EtOH)
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

(R,R)-(+)-Bis(a-methylbenzyl)amine hydrochloride is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically pure compounds, which is crucial in pharmaceuticals and agrochemicals.
  • Catalysis: It is employed in catalytic processes, particularly in the synthesis of complex organic molecules, enhancing reaction efficiency and selectivity.
  • Pharmaceutical Development: This chemical plays a significant role in drug formulation, particularly in developing medications that require specific stereochemistry for efficacy.
  • Research in Organocatalysis: It is used in studies exploring organocatalytic reactions, providing insights into new methodologies for organic synthesis.
  • Material Science: The compound is explored in the development of new materials, particularly those requiring specific molecular interactions for improved performance in applications like sensors and coatings.

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