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Catalog Number:
39650
CAS Number:
108149-60-6
( S )-(-)-3- tert -butoxycarbonyl-4-méthoxycarbonyl-2,2-diméthyl-1,3-oxazolidine
Purity:
≥ 98,5 % (pureté chirale)
Synonym(s):
( S )-(-)-3-Boc-4-méthoxycarbonyl-2,2-diméthyl-1,3-oxazolidine, Méthyl( S )-(-)-3- tert -butoxycarbonyl-2,2-diméthyl-4-oxazolidinecarboxylate
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Taille
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Informations sur le produit
Numéro CAS 
108149-60-6
Formule moléculaire
C 12 H 215
Poids moléculaire 
0
Indice de réfraction 
n20D 1.44
Rotation optique 
[α] 20 D = 55 ± 2 ° (C = 1,3 dans le chloroforme)
Informations générales
Numéro CAS 
108149-60-6
Formule moléculaire
C 12 H 215
Poids moléculaire 
0
Indice de réfraction 
n20D 1.44
Rotation optique 
[α] 20 D = 55 ± 2 ° (C = 1,3 dans le chloroforme)
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 
-
Applications

(S)-(-)-3-tert-Butoxycarbonyl-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs that target neurological disorders.
  • Peptide Synthesis: It is used in the solid-phase synthesis of peptides, enhancing the efficiency and yield of the process, which is crucial for producing therapeutic proteins.
  • Chiral Auxiliary: The compound acts as a chiral auxiliary in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds, which are vital in drug formulation.
  • Research in Organic Chemistry: It provides a versatile framework for the exploration of new synthetic pathways and methodologies, aiding researchers in discovering novel compounds.
  • Bioconjugation Techniques: This chemical is employed in bioconjugation strategies, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutics.

Citations