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Catalog Number:
01382
CAS Number:
56675-37-7
Boc-β-(2-thiényl)-L-alanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Ala-3-(2-thiényl)-OH, ( S - N -Boc-2-thiénylalanine
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Informations sur le produit

Boc-b-(2-thienyl)-L-alanine is a versatile amino acid derivative that serves as a valuable building block in peptide synthesis and medicinal chemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers involved in the development of novel therapeutics. Its unique thiophene moiety contributes to its potential in creating compounds with enhanced biological activity, particularly in the fields of drug discovery and development.

Researchers can leverage Boc-b-(2-thienyl)-L-alanine in the synthesis of bioactive peptides, where its structural properties can facilitate the design of inhibitors or modulators for various biological targets. The compound's compatibility with standard coupling reagents and its ability to undergo selective deprotection make it an attractive option for those looking to streamline their synthetic processes. With its promising applications in pharmaceuticals and biochemistry, Boc-b-(2-thienyl)-L-alanine stands out as a key component for innovative research and development.

Numéro CAS 
56675-37-7
Formule moléculaire
C 12 H 17 NON 4 S
Poids moléculaire 
271.3
Rotation optique 
=+24°±1,5°(c=2% EtOH)
Informations générales
Numéro CAS 
56675-37-7
Formule moléculaire
C 12 H 17 NON 4 S
Poids moléculaire 
271.3
Rotation optique 
=+24°±1,5°(c=2% EtOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-b-(2-thienyl)-L-alanine 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 bioactive compounds that can be used in pharmaceuticals.
  • Drug Development: Its unique structure allows for the creation of novel drug candidates, especially in the field of cancer research, where compounds with thiophene rings have shown promising activity.
  • Bioconjugation: The compound can be used in bioconjugation techniques, enabling the attachment of biomolecules to therapeutic agents, enhancing their efficacy and targeting capabilities.
  • Research in Neuroscience: It has potential applications in studying neurotransmitter systems due to its ability to mimic amino acids, which can help in the development of neuroactive drugs.
  • Material Science: The compound is also explored in the development of advanced materials, particularly in organic electronics and sensors, owing to its conductive properties.

Citations