Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
04025
CAS Number:
19391-35-6
Éster bencílico de Boc-L-tirosina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Tyr-OBzl
Documents
$67.60 /1G
Tamaño
Request Bulk Quote
Información del producto

Boc-L-tyrosine benzyl ester is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a benzyl ester group that enhances its lipophilicity, making it an ideal candidate for various applications in organic synthesis and medicinal chemistry. Its unique structure allows for the protection of the amino group, facilitating the formation of complex peptides while maintaining the integrity of the tyrosine side chain. Researchers often leverage Boc-L-tyrosine benzyl ester in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial for achieving desired biological activities.

In addition to its role in peptide synthesis, Boc-L-tyrosine benzyl ester serves as a valuable building block in the creation of bioactive compounds and drug candidates. Its ability to undergo selective reactions enables chemists to explore diverse modifications, leading to the discovery of novel therapeutic agents. With its favorable properties and practical applications, Boc-L-tyrosine benzyl ester stands out as an essential tool for researchers and industry professionals aiming to innovate in the fields of biochemistry and pharmaceuticals.

Número CAS
19391-35-6
Fórmula molecular
C 21 H 25 N.º 5
Peso molecular
371.44
Número MDL
MFCD00190840
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
19391-35-6
Fórmula molecular
C 21 H 25 N.º 5
Peso molecular
371.44
Número MDL
MFCD00190840
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Boc-L-tyrosine benzyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create specific sequences for studying protein interactions and functions.
  • Drug Development: It is used in the development of pharmaceutical compounds, particularly in creating prodrugs that improve the bioavailability of therapeutic agents.
  • Bioconjugation: The chemical's reactive groups facilitate bioconjugation processes, enabling the attachment of drugs or imaging agents to biomolecules for targeted therapies.
  • Research in Neuroscience: Due to its structural similarity to neurotransmitters, it aids in the study of neurochemical pathways and the development of treatments for neurological disorders.
  • Cosmetic Formulations: Its properties are leveraged in cosmetic chemistry to enhance formulations aimed at skin health, particularly in products targeting aging and hydration.

Citas