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Catalog Number:
01351
CAS Number:
13726-84-6
Ester γ- tert -butylique de l'acide boc-L-glutamique
Purity:
≥ 99,5 % (pureté chirale)
Synonym(s):
Boc-L-Glu(OtBu)-OH, Ester 5- tert -butylique de l'acide boc-L-glutamique
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Informations sur le produit

Boc-L-glutamic acid g-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This protected form of L-glutamic acid offers enhanced stability and solubility, making it an ideal choice for researchers looking to develop complex peptides and proteins. Its unique tert-butyl ester groups provide excellent protection against unwanted reactions during synthesis, allowing for more precise control over the final product. This compound is particularly beneficial in the development of drug candidates, where the integrity of the amino acid structure is crucial for biological activity.

In addition to its role in peptide synthesis, Boc-L-glutamic acid g-tert-butyl ester is also employed in the production of various bioactive compounds and can serve as a building block in the synthesis of pharmaceuticals and agrochemicals. Researchers appreciate its ease of use and compatibility with a range of coupling reagents, which streamlines the synthesis process. The compound's favorable properties not only enhance yield but also improve the overall efficiency of synthetic routes, making it a valuable asset in both academic and industrial laboratories.

Numéro CAS 
13726-84-6
Formule moléculaire
C 14 H 256
Poids moléculaire 
303.4
Point de fusion 
108 - 118 ?C
Rotation optique 
[a] 20 D = -9,5 ± 1 ° (C=2 dans MeOH)
Informations générales
Numéro CAS 
13726-84-6
Formule moléculaire
C 14 H 256
Poids moléculaire 
303.4
Point de fusion 
108 - 118 ?C
Rotation optique 
[a] 20 D = -9,5 ± 1 ° (C=2 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Boc-L-glutamic acid g-tert-butyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it plays a crucial role in the design of prodrugs, which enhance the bioavailability of active pharmaceutical ingredients, improving therapeutic outcomes.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in developing targeted drug delivery systems.
  • Research in Neuroscience: It is applied in the synthesis of neurotransmitter analogs, aiding in the study of neurological pathways and potential treatments for neurodegenerative diseases.
  • Material Science: The compound is also explored in creating novel polymers and materials with specific properties, contributing to advancements in fields like coatings and adhesives.

Citations