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Catalog Number:
23124
CAS Number:
76936-87-3
N- (1-pirenil)yodoacetamida
Purity:
≥ 97%
Documents
$113.87 /25 mg
Tamaño
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Información del producto

N-(1-Pyrenyl)iodoacetamide is a versatile compound widely recognized for its unique properties and applications in various fields, particularly in organic synthesis and materials science. This compound features a pyrene moiety, which is known for its excellent photophysical properties, making it an ideal candidate for use in fluorescence studies and as a fluorescent probe. Its iodoacetamide functional group enhances its reactivity, allowing for easy conjugation with biomolecules, which is particularly beneficial in bioconjugation and labeling applications. Researchers have successfully utilized N-(1-Pyrenyl)iodoacetamide in the development of novel fluorescent sensors and in the study of protein interactions, showcasing its potential in biochemical research.

In addition to its applications in research, N-(1-Pyrenyl)iodoacetamide is also being explored for its potential in the development of advanced materials, such as organic light-emitting diodes (OLEDs) and photovoltaic devices. Its ability to form stable complexes with various substrates enhances its utility in creating functional materials with tailored properties. With its unique combination of reactivity and photophysical characteristics, N-(1-Pyrenyl)iodoacetamide stands out as a valuable tool for researchers and industry professionals seeking innovative solutions in chemical synthesis and material development.

Número CAS
76936-87-3
Fórmula molecular
C 18 H 12 NOI
Peso molecular
385.2
Número MDL
MFCD00467798
Punto de fusión
225 - 227 °C (descenso)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
76936-87-3
Fórmula molecular
C 18 H 12 NOI
Peso molecular
385.2
Número MDL
MFCD00467798
Punto de fusión
225 - 227 °C (descenso)
Condiciones
Conservar entre 0 y 8 °C.
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

N-(1-Pyrenyl)iodoacetamide is widely utilized in research focused on:

  • Fluorescent Probes: This compound serves as a fluorescent probe in biochemical assays, allowing researchers to track cellular processes and interactions with high sensitivity.
  • Drug Development: It is used in the development of new pharmaceuticals, particularly in targeting specific proteins, enhancing the efficacy of drug candidates.
  • Material Science: The compound is incorporated into polymer matrices to create materials with enhanced optical properties, useful in sensors and display technologies.
  • Bioconjugation: It facilitates bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other compounds, which is essential in diagnostics and therapeutic applications.
  • Environmental Monitoring: N-(1-Pyrenyl)iodoacetamide is applied in environmental studies to detect and quantify pollutants, providing valuable data for ecological assessments.

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