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Catalog Number:
03216
CAS Number:
69610-40-8
Boc-L-prolinol
Purity:
≥ 98% (CG)
Synonym(s):
Boc-Pro-ol
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$20.63 /1G
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Informations sur le produit

Boc-L-prolinol is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This amino alcohol derivative features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and reactivity in various chemical reactions. Its unique structure allows for the synthesis of complex molecules, making it an essential building block in the development of peptide-based therapeutics and other bioactive compounds. Researchers appreciate Boc-L-prolinol for its ability to facilitate the formation of peptide bonds and its role in asymmetric synthesis, contributing to the creation of enantiomerically pure products.

In addition to its applications in drug discovery, Boc-L-prolinol is also employed in the synthesis of chiral ligands and catalysts, which are crucial in enantioselective reactions. Its favorable properties, such as solubility in organic solvents and compatibility with various reaction conditions, make it a preferred choice for chemists seeking reliable and efficient reagents. With its broad range of applications, Boc-L-prolinol stands out as a valuable asset in both academic and industrial settings.

Numéro CAS 
69610-40-8
Formule moléculaire
C 10 H 19 NON 3
Poids moléculaire 
201.25
Point de fusion 
58-66 °C
Rotation optique 
[a] D 25 = -46,0 à -52,0º (C = 1,3 dans CHCl 3 )
Informations générales
Numéro CAS 
69610-40-8
Formule moléculaire
C 10 H 19 NON 3
Poids moléculaire 
201.25
Point de fusion 
58-66 °C
Rotation optique 
[a] D 25 = -46,0 à -52,0º (C = 1,3 dans CHCl 3 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-L-prolinol is widely utilized in research focused on:

  • Synthesis of Peptides: This compound serves as a versatile building block in peptide synthesis, allowing chemists to create complex structures with improved stability and bioactivity.
  • Pharmaceutical Development: Its unique properties make it valuable in drug formulation, particularly in designing prodrugs that enhance solubility and bioavailability, leading to more effective medications.
  • Chiral Auxiliary in Organic Synthesis: Boc-L-prolinol acts as a chiral auxiliary, facilitating asymmetric synthesis. This is crucial in producing enantiomerically pure compounds, which are essential in the pharmaceutical industry.
  • Research in Catalysis: It is used in catalytic processes, particularly in the development of new catalysts that can improve reaction efficiency and selectivity in organic reactions.
  • Bioconjugation Techniques: The compound is employed in bioconjugation, where it helps link biomolecules to therapeutic agents, enhancing targeted delivery systems in drug development.

Citations