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Catalog Number:
41318
CAS Number:
6129-15-3
( R )-(+)- N -(1-Feniletil)maleimida
Purity:
≥ 97% (ensayo)
Synonym(s):
1-[(1 R )-1-Feniletil]-2,5-dihidro-1 H -pirrol-2,5-diona
Documents
$66.80 /250 mg
Tamaño
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Información del producto

(R)-(+)-N-(1-Phenylethyl)maleimide is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This chiral maleimide derivative is particularly valued for its ability to selectively react with thiols, making it an essential reagent in the development of bioconjugates and drug delivery systems. Its unique structure allows for the formation of stable adducts, which are crucial in the design of targeted therapies and diagnostic agents. Researchers have successfully utilized this compound in the synthesis of peptide-based therapeutics and in the creation of functionalized materials for advanced applications in nanotechnology.

In addition to its synthetic utility, (R)-(+)-N-(1-Phenylethyl)maleimide exhibits promising properties in the field of polymer chemistry, where it can be employed as a building block for the preparation of functional polymers with tailored properties. Its ability to facilitate cross-linking reactions enhances the mechanical and thermal stability of polymeric materials, making it a valuable asset in the production of high-performance composites. With its broad range of applications and benefits, this compound is an excellent choice for researchers and industry professionals looking to innovate in their respective fields.

Número CAS
6129-15-3
Fórmula molecular
C12H11NO2
Peso molecular
201.22
Número MDL
MFCD00674054
Densidad
1,138 g/mL a 25 °C (Lit.)
Punto de ebullición
110 - 115 °C / 0,004 mmHg (Literatura)
Índice de refracción
n20D 1.556 (Literatura)
Rotación óptica
[α] 24 D = 61 ± 1 ° (C = 2 en EtOH)
Condiciones
Tienda en RT
Información general
Número CAS
6129-15-3
Fórmula molecular
C12H11NO2
Peso molecular
201.22
Número MDL
MFCD00674054
Densidad
1,138 g/mL a 25 °C (Lit.)
Punto de ebullición
110 - 115 °C / 0,004 mmHg (Literatura)
Índice de refracción
n20D 1.556 (Literatura)
Rotación óptica
[α] 24 D = 61 ± 1 ° (C = 2 en 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
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Aplicaciones

(R)-(+)-N-(1-Phenylethyl)maleimide is widely utilized in research focused on

  • Organic Synthesis: This compound serves as a versatile intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Chiral Catalysis: Its chiral nature makes it an excellent candidate for asymmetric synthesis, allowing researchers to produce enantiomerically pure compounds more efficiently than with non-chiral alternatives.
  • Polymer Chemistry: It is used in the formulation of specialty polymers, enhancing properties such as thermal stability and mechanical strength, which are crucial in materials science.
  • Bioconjugation: The compound can be employed in bioconjugation techniques, aiding in the development of targeted drug delivery systems and diagnostic tools in the biomedical field.
  • Fluorescent Probes: It is also utilized in creating fluorescent probes for biological imaging, providing researchers with valuable tools for studying cellular processes.

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