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Catalog Number:
07268
CAS Number:
132286-77-2
Ester β-allylique de l'acide boc-L-aspartique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Asp(OAll)-OH
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Informations sur le produit

Boc-L-aspartic acid-b-allyl ester is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This derivative of aspartic acid features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and reactivity during various chemical reactions. Its unique structure allows for selective modifications, making it an essential building block in the development of bioactive peptides and pharmaceuticals. Researchers often leverage its properties to create compounds with improved bioavailability and targeted therapeutic effects, particularly in the fields of drug discovery and development.

In addition to its applications in peptide synthesis, Boc-L-aspartic acid-b-allyl ester serves as a valuable intermediate in the production of agrochemicals and other specialty chemicals. Its ability to undergo various transformations while maintaining structural integrity makes it an attractive option for chemists looking to innovate in their formulations. With its proven track record in enhancing the efficacy of therapeutic agents, this compound is an excellent choice for professionals seeking reliable and effective solutions in their research and development endeavors.

Numéro CAS 
132286-77-2
Formule moléculaire
C 12 H 196
Poids moléculaire 
273.3
Point de fusion 
44 - 50 °C
Rotation optique 
[a] D 25 = -28,8 ± 2 º (C = 1 dans DMF)
Informations générales
Numéro CAS 
132286-77-2
Formule moléculaire
C 12 H 196
Poids moléculaire 
273.3
Point de fusion 
44 - 50 °C
Rotation optique 
[a] D 25 = -28,8 ± 2 º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-L-aspartic acid-b-allyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of pharmaceuticals and biologically active compounds.
  • Drug Development: Its unique structure allows for the modification of drug candidates, enhancing their bioavailability and therapeutic efficacy, which is crucial in the pharmaceutical industry.
  • Bioconjugation: The allyl group facilitates bioconjugation processes, enabling the attachment of biomolecules to therapeutic agents, which is important in targeted drug delivery systems.
  • Research in Neuroscience: It is used in studies related to neurotransmitter pathways, particularly in the synthesis of compounds that mimic or inhibit aspartate receptors, aiding in neurological research.
  • Polymer Chemistry: The compound can be incorporated into polymer matrices, enhancing properties such as solubility and reactivity, which is beneficial in materials science applications.

Citations