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Catalog Number:
37518
CAS Number:
40648-92-8
( S , S -(-)-Clorhidrato de bis(α-metilbencil)amina
Purity:
≥ 98 % (T) (HPLC)
Synonym(s):
Clorhidrato de (-)-bis[( S -1-feniletil]amina, Clorhidrato de (-)-bis[( S -α-metilbencil]amina
Documents
$392.19 /5G
Tamaño
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Información del producto

(S,S)-(-)-Bis(a-methylbenzyl)amine hydrochloride is a versatile compound widely utilized in various fields, particularly in organic synthesis and pharmaceutical research. This chiral amine is recognized for its ability to act as a ligand in asymmetric synthesis, making it invaluable for producing enantiomerically pure compounds. Its unique structure allows for effective interactions in catalytic processes, enhancing reaction efficiency and selectivity. Researchers have leveraged this compound in the development of novel pharmaceuticals, particularly in the synthesis of complex molecules where chirality is crucial.

Additionally, (S,S)-(-)-Bis(a-methylbenzyl)amine hydrochloride serves as a building block in the creation of advanced materials and fine chemicals. Its application extends to the production of agrochemicals and specialty chemicals, where its properties can improve product performance and stability. With its proven track record in enhancing reaction pathways and yielding high-purity products, this compound stands out as a preferred choice for professionals seeking reliable and effective solutions in their chemical processes.

Número CAS
40648-92-8
Fórmula molecular
C16H19N · HCl
Peso molecular
261.79
Número MDL
MFCD00216671
Rotación óptica
[α]20 D = -70 a -76 ° (C=3, EtOH)
Condiciones
Tienda en RT
Información general
Número CAS
40648-92-8
Fórmula molecular
C16H19N · HCl
Peso molecular
261.79
Número MDL
MFCD00216671
Rotación óptica
[α]20 D = -70 a -76 ° (C=3, EtOH)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

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

  • Synthesis of Pharmaceuticals: This compound serves as a chiral auxiliary in the synthesis of various pharmaceuticals, enhancing the production of enantiomerically pure drugs, which is crucial for efficacy and safety in medicine.
  • Asymmetric Catalysis: It plays a significant role in asymmetric catalysis, helping chemists create compounds with specific configurations, which is essential in developing new materials and drugs.
  • Research in Organocatalysis: This chemical is used in organocatalytic reactions, providing a more environmentally friendly alternative to traditional metal catalysts, reducing waste and improving sustainability in chemical processes.
  • Development of Agrochemicals: It is applied in the formulation of agrochemicals, aiding in the design of more effective pesticides and herbicides that target specific pests while minimizing environmental impact.
  • Chiral Separation Techniques: The compound is utilized in chiral separation methods, allowing researchers to isolate and purify enantiomers, which is vital for both pharmaceutical development and quality control.

Citas