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Catalog Number:
05048
CAS Number:
215190-29-7
Fmoc-4-(3-carboxyméthyl-2-céto-one-benzimidazolyl)pipéridine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-Ckbp-OH
Documents
$120.88 /100 mg
Taille
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Informations sur le produit

Fmoc-4-(3-carboxymethyl-2-keto-one-benzimidazolyl)piperidine is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its structure includes a benzimidazole moiety, known for its biological activity, making it particularly valuable in drug development and research. The carboxymethyl and keto functionalities enhance its reactivity and solubility, facilitating its application in various organic synthesis processes.

Researchers and industry professionals can leverage this compound for the development of novel therapeutic agents, especially in the fields of oncology and infectious diseases. Its ability to form stable peptide bonds and its compatibility with various coupling reagents make it an excellent choice for synthesizing complex peptide sequences. Additionally, the unique properties of this compound allow for modifications that can lead to improved pharmacological profiles, making it a preferred option in pharmaceutical research and development.

Numéro CAS 
215190-29-7
Formule moléculaire
C29H27N3O5
Poids moléculaire 
497.54
Informations générales
Numéro CAS 
215190-29-7
Formule moléculaire
C29H27N3O5
Poids moléculaire 
497.54
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

Fmoc-4-(3-carboxymethyl-2-keto-one-benzimidazolyl)piperidine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective formation of peptide bonds while preventing unwanted reactions.
  • Drug Development: Its unique structure is beneficial in the design of novel pharmaceuticals, particularly in targeting specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound can be used to create bioconjugates, linking biomolecules to drugs or imaging agents, which is crucial in targeted therapy and diagnostics.
  • Material Science: It finds applications in developing advanced materials, such as polymers and nanomaterials, that require specific functional groups for enhanced properties.
  • Research in Cancer Therapy: The compound's ability to interact with biological targets makes it valuable in cancer research, where it can help in the development of targeted treatments.

Citations