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Catalog Number:
01699
CAS Number:
5497-76-7
Clorhidrato de éster terc -butílico de L-prolina
Purity:
97,5 - 102,5% (Determinación por titulación)
Synonym(s):
L-Pro-OtBu·HCl, ( Clorhidrato de éster terc -butílico del ácido S -pirrolidina-2-carboxílico
Documents
$67.60 /5G
Tamaño
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Información del producto

L-Proline tert-butyl ester hydrochloride is a versatile compound widely utilized in the synthesis of peptides and pharmaceuticals. This derivative of proline offers enhanced solubility and stability, making it an ideal choice for researchers and industry professionals engaged in organic synthesis and drug development. Its unique structure allows for easier incorporation into various chemical reactions, particularly in the formation of peptide bonds, which are crucial in the development of biologically active compounds.

In addition to its applications in peptide synthesis, L-Proline tert-butyl ester hydrochloride serves as a valuable chiral auxiliary in asymmetric synthesis, facilitating the production of enantiomerically pure compounds. This characteristic is particularly beneficial in the pharmaceutical industry, where the efficacy and safety of drugs can depend on their stereochemistry. With its favorable properties and practical applications, this compound is an essential tool for chemists aiming to innovate and optimize their synthetic pathways.

Número CAS
5497-76-7
Fórmula molecular
C9H17NO2 · HCl
Peso molecular
207.7
Número MDL
MFCD00153459
Punto de fusión
91 - 110 °C
Rotación óptica
[a] 20 D = -33 ± 2,5 ° (C=2 en EtOH)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
5497-76-7
Fórmula molecular
C9H17NO2 · HCl
Peso molecular
207.7
Número MDL
MFCD00153459
Punto de fusión
91 - 110 °C
Rotación óptica
[a] 20 D = -33 ± 2,5 ° (C=2 en EtOH)
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 tert-butyl ester hydrochloride 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 in drug development and biochemistry.
  • Pharmaceutical Applications: It is used in the formulation of various pharmaceuticals, particularly in creating proline derivatives that can enhance drug efficacy.
  • Biochemical Research: Researchers employ this compound to study protein folding and enzyme activity, providing insights into biological processes and disease mechanisms.
  • Chiral Catalysis: Its chiral nature makes it an excellent candidate in asymmetric synthesis, allowing for the production of enantiomerically pure compounds, which are essential in the pharmaceutical industry.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential to improve skin hydration and elasticity, making it a beneficial ingredient in skincare products.

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