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Catalog Number:
39478
CAS Number:
86695-06-9
( R )-(+)-2-Amino-3-metil-1,1-difenil-1-butanol
Purity:
≥ 99 % (HPLC quiral)
Documents
$95.94 /1G
Tamaño
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Información del producto

(R)-(+)-2-Amino-3-methyl-1,1-diphenyl-1-butanol is a chiral amino alcohol that plays a significant role in the synthesis of various pharmaceuticals and agrochemicals. This compound is particularly valued for its ability to act as a chiral auxiliary in asymmetric synthesis, facilitating the production of enantiomerically pure compounds, which are crucial in the development of effective drugs. Its unique structure allows for enhanced selectivity in reactions, making it an essential tool for researchers in medicinal chemistry and organic synthesis.

In addition to its applications in drug development, (R)-(+)-2-Amino-3-methyl-1,1-diphenyl-1-butanol is also utilized in the production of fine chemicals and specialty materials. Its versatility and effectiveness in catalyzing reactions make it a preferred choice for professionals seeking to optimize their synthetic pathways. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, ensuring reliable results in various applications.

Número CAS
86695-06-9
Fórmula molecular
C 17 H 21 NO
Peso molecular
255.36
Número MDL
MFCD01318247
Punto de fusión
96 - 101 °C
Rotación óptica
[α]20 D = 130 - 145 ° (C=1 en CHCl 3 )
Condiciones
Tienda en RT
Información general
Número CAS
86695-06-9
Fórmula molecular
C 17 H 21 NO
Peso molecular
255.36
Número MDL
MFCD01318247
Punto de fusión
96 - 101 °C
Rotación óptica
[α]20 D = 130 - 145 ° (C=1 en CHCl 3 )
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

(R)-(+)-2-Amino-3-methyl-1,1-diphenyl-1-butanol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a chiral building block in the synthesis of various pharmaceuticals, enhancing the efficacy and selectivity of drug formulations.
  • Chiral Catalysis: It is employed as a catalyst in asymmetric synthesis, allowing for the production of enantiomerically pure compounds, which is crucial in the development of effective medications.
  • Biochemical Research: Researchers use it to study enzyme interactions and mechanisms, providing insights into metabolic pathways and potential therapeutic targets.
  • Material Science: The compound is explored for its potential in creating advanced materials, such as polymers with specific optical properties, beneficial for electronics and photonics.
  • Analytical Chemistry: It is utilized in chiral chromatography, aiding in the separation and analysis of enantiomers in various samples, which is essential for quality control in the pharmaceutical industry.

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