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Catalog Number:
11835
CAS Number:
259221-91-5
Ester γ-allylique de l'acide boc-D-glutamique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-D-Glu(O11)-OH, Ester 5-allylique de l'acide boc-D-glutamique
Documents
$36.65 /1G
Taille
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Informations sur le produit

Boc-D-glutamic acid g-allyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This derivative of glutamic acid features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity in various chemical reactions. Its unique structure allows for selective modifications, making it an essential building block in the development of bioactive peptides and drug candidates. Researchers appreciate its ability to facilitate the introduction of functional groups, enabling the design of compounds with tailored properties for specific applications in medicinal chemistry.

In addition to its role in peptide synthesis, Boc-D-glutamic acid g-allyl ester is also employed in the production of advanced materials and as an intermediate in organic synthesis. Its compatibility with various coupling reactions and ease of handling make it a preferred choice for professionals in the pharmaceutical and biotechnology sectors. With its potential to streamline the synthesis of complex molecules, this compound stands out as a valuable asset for researchers aiming to innovate in drug development and related fields.

Numéro CAS 
259221-91-5
Formule moléculaire
C 13 H 216
Poids moléculaire 
287.4
Point de fusion 
43-49 ºC
Rotation optique 
[a] D 20 = + 10 ± 2 º (C=1 dans MeOH)
Informations générales
Numéro CAS 
259221-91-5
Formule moléculaire
C 13 H 216
Poids moléculaire 
287.4
Point de fusion 
43-49 ºC
Rotation optique 
[a] D 20 = + 10 ± 2 º (C=1 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-D-glutamic acid g-allyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of bioactive compounds and pharmaceuticals.
  • Drug Development: Its unique structure allows for modifications that enhance the solubility and bioavailability of drug candidates, making it valuable in medicinal chemistry.
  • Bioconjugation: The allyl group can be used for selective reactions, facilitating the attachment of biomolecules to surfaces or other compounds, which is crucial in creating targeted therapies.
  • Research in Neuroscience: This compound can be utilized in studies related to neurotransmitter functions, potentially leading to advancements in understanding neurological disorders.
  • Material Science: Its properties enable the development of novel materials with specific functionalities, such as hydrogels or coatings, which can be applied in various industrial sectors.

Citations