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Catalog Number:
04985
CAS Number:
144069-67-0
Acide boc-L-indoline-2-carboxylique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-L-IDC-OH, Acide boc-(2 S -indoline carboxylique
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Informations sur le produit

Boc-L-indoline-2-carboxylic acid is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This compound, characterized by its unique structure, serves as a valuable building block for the development of various pharmaceuticals and bioactive molecules. Its Boc (tert-butyloxycarbonyl) protecting group enhances its stability and solubility, making it an ideal candidate for peptide synthesis and other complex organic reactions. Researchers often leverage this compound in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties.

In addition to its role in synthetic chemistry, Boc-L-indoline-2-carboxylic acid is recognized for its potential applications in drug discovery and development. Its ability to facilitate the formation of intricate molecular architectures allows for the exploration of new therapeutic agents. The compound's favorable properties, such as its ease of handling and compatibility with various reaction conditions, make it a preferred choice among chemists and researchers seeking to innovate in the pharmaceutical landscape.

Numéro CAS 
144069-67-0
Formule moléculaire
C 14 H 17 NON 4
Poids moléculaire 
263.3
Rotation optique 
[a] D 20 = -81 ± 2º (C = 1,5 dans CHCl3 ou DMF)
Informations générales
Numéro CAS 
144069-67-0
Formule moléculaire
C 14 H 17 NON 4
Poids moléculaire 
263.3
Rotation optique 
[a] D 20 = -81 ± 2º (C = 1,5 dans CHCl3 ou DMF)
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-L-indoline-2-carboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in creating modified amino acids that enhance the stability and bioactivity of therapeutic peptides.
  • Drug Development: It is employed in the pharmaceutical industry for the development of novel drug candidates, especially in targeting specific biological pathways, due to its unique structural properties.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving their efficacy and targeting capabilities.
  • Research in Neuroscience: Its derivatives are investigated for potential applications in neuroscience, particularly in the study of neurotransmitter systems and neuroprotective agents.
  • Material Science: Boc-L-indoline-2-carboxylic acid is also explored in the development of advanced materials, including polymers and coatings, due to its ability to enhance material properties.

Citations