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Catalog Number:
06203
CAS Number:
7369-91-7
L-Prolina 4-nitroanilida
Purity:
≥ 98 % (HPLC)
Synonym(s):
L-Pro-pNA, Ácido ( S )-pirrolidina-2-carboxílico 4-nitroanilida
Documents
$70.00 /100 mg
Tamaño
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Información del producto

L-Proline 4-nitroanilide is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This amino acid derivative features a unique nitrophenyl group, enhancing its reactivity and making it an essential building block in the synthesis of various bioactive molecules. Its structural properties allow it to serve as a key intermediate in the development of peptide-based drugs and enzyme inhibitors, providing researchers with a valuable tool for exploring new therapeutic avenues.

In addition to its synthetic applications, L-Proline 4-nitroanilide is also employed in the study of protein folding and stability, contributing to advancements in understanding complex biological processes. Its ability to participate in various chemical reactions, including coupling and acylation, positions it as a preferred choice for chemists seeking efficient pathways to synthesize novel compounds. With its unique properties and broad applicability, L-Proline 4-nitroanilide stands out as a significant asset in both academic and industrial research settings.

Número CAS
7369-91-7
Fórmula molecular
C11H13N3O3
Peso molecular
235.15
Número MDL
MFCD00037865
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
7369-91-7
Fórmula molecular
C11H13N3O3
Peso molecular
235.15
Número MDL
MFCD00037865
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

L-Proline 4-nitroanilide is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, which are crucial for developing new drugs and therapeutic agents.
  • Biochemical Assays: It is commonly used in enzyme assays to study protease activity, helping researchers understand enzyme mechanisms and develop inhibitors.
  • Fluorescent Probes: The compound can be modified to create fluorescent probes, enhancing imaging techniques in biological research and diagnostics.
  • Pharmaceutical Development: Its unique properties make it a candidate for designing new pharmaceuticals, particularly in targeting specific biological pathways.
  • Material Science: L-Proline 4-nitroanilide is explored in the development of novel materials, including polymers that exhibit improved mechanical properties.

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