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Catalog Number:
41616
CAS Number:
87219-29-2
( S )-β-(Carbobenzoxiamino)-γ-butirolactona
Purity:
≥ 98 % (HPLC)
Synonym(s):
( S )-β-(Cbz-amino)-γ-butirolactona, ( S )-4-(Carbobenzoxiamino)tetrahidrofuran-2-ona, ( S )-4-(Cbz-amino)tetrahidrofurano-2-ona, ( S )-Tetrahidro-5-oxo-3-furanilcarbamato de bencilo
Documents
$64.00 /1G
Tamaño
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Información del producto

(S)-b-(Carbobenzoxyamino)-g-butyrolactone is a versatile compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This compound, also known as benzyl N-[(3S)-5-oxooxolan-3-yl]carbamate, features a unique structure that enhances its reactivity and selectivity in chemical reactions. Its ability to act as a chiral building block makes it particularly valuable in the development of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for creating effective and safe medications.

Researchers and industry professionals appreciate (S)-b-(Carbobenzoxyamino)-g-butyrolactone for its role in the synthesis of amino acids and peptide derivatives, which are essential in drug development and biochemistry. The compound's stability and compatibility with various reaction conditions further expand its applicability, making it an ideal choice for those looking to innovate in drug formulation and synthesis processes. Its unique properties not only streamline production but also enhance the overall efficiency of chemical processes, providing a competitive edge in research and development.

Número CAS
87219-29-2
Fórmula molecular
C12H13NO4
Peso molecular
235.24
Número MDL
MFCD00216569
Punto de fusión
103 - 107 °C
Rotación óptica
[a]20D = -57 a -53 ° (C = 1 en CHCl3)
Condiciones
Tienda en RT
Información general
Número CAS
87219-29-2
Fórmula molecular
C12H13NO4
Peso molecular
235.24
Número MDL
MFCD00216569
Punto de fusión
103 - 107 °C
Rotación óptica
[a]20D = -57 a -53 ° (C = 1 en CHCl3)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(S)-b-(Carbobenzoxyamino)-g-butyrolactone is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders.
  • Peptide Synthesis: It is employed in the formation of peptide bonds, making it valuable in the production of peptides for therapeutic applications, including antibiotics and hormones.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Research in Organic Chemistry: It acts as a building block in organic synthesis, facilitating the creation of complex molecules and contributing to advancements in synthetic methodologies.
  • Material Science: This chemical is explored in the development of new materials, particularly in creating polymers with specific properties for use in coatings and adhesives.

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