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Catalog Number:
39650
CAS Number:
108149-60-6
( S )-(-)-3- terc -Butoxicarbonil-4-metoxicarbonil-2,2-dimetil-1,3-oxazolidina
Purity:
≥ 98,5 % (pureza quiral)
Synonym(s):
( S )-(-)-3-Boc-4-metoxicarbonil-2,2-dimetil-1,3-oxazolidina, Metil( S )-(-)-3- terc -Butoxicarbonil-2,2-dimetil-4-oxazolidinacarboxilato
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Documents
$43.87 /1G
Tamaño
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Información del producto
Número CAS
108149-60-6
Fórmula molecular
C12H21NO5
Peso molecular
0
Número MDL
MFCD00192279
Densidad
1,08 g/mL a 25 °C
Punto de ebullición
101 - 102 °C / 2 mmHg (Literatura)
Índice de refracción
n20D 1,44
Rotación óptica
[α] 20 D = 55 ± 2 ° (C = 1,3 en cloroformo)
Condiciones
Tienda en RT
Información general
Número CAS
108149-60-6
Fórmula molecular
C12H21NO5
Peso molecular
0
Número MDL
MFCD00192279
Densidad
1,08 g/mL a 25 °C
Punto de ebullición
101 - 102 °C / 2 mmHg (Literatura)
Índice de refracción
n20D 1,44
Rotación óptica
[α] 20 D = 55 ± 2 ° (C = 1,3 en cloroformo)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(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.

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