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Catalog Number:
41308
CAS Number:
104597-98-0
Méthyl ( S )-(-)- N -Z-aziridine-2-carboxylate
Purity:
≥ 96 % (dosage)
Synonym(s):
( S )-1-Benzyl 2-méthyl aziridine-1,2-dicarboxylate, 1-Benzyl 2-méthyl ( S )-aziridine-1,2-dicarboxylate
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Informations sur le produit

Methyl (S)-(-)-N-Z-aziridine-2-carboxylate is a versatile compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This chiral aziridine derivative is particularly valued for its ability to serve as a building block in the development of biologically active molecules. Its unique structure allows for the introduction of functional groups, making it an essential intermediate in the production of complex organic compounds. Researchers and industry professionals appreciate its role in asymmetric synthesis, where it can facilitate the creation of enantiomerically pure products, crucial for drug development.

In addition to its applications in medicinal chemistry, Methyl (S)-(-)-N-Z-aziridine-2-carboxylate is also employed in the formulation of agrochemicals, enhancing the efficacy of crop protection agents. Its stability and reactivity make it an attractive option for those looking to innovate in the fields of pharmaceuticals and agriculture. With its potential to streamline synthesis processes and improve product performance, this compound stands out as a valuable asset for researchers and manufacturers alike.

Numéro CAS 
104597-98-0
Formule moléculaire
C 12 H 13 NON 4
Poids moléculaire 
235.24
Indice de réfraction 
n20D 1.519 (Lit.)
Rotation optique 
[α] 20 D = -30 à -22 ° (C = 1 dans le toluène)
Informations générales
Numéro CAS 
104597-98-0
Formule moléculaire
C 12 H 13 NON 4
Poids moléculaire 
235.24
Indice de réfraction 
n20D 1.519 (Lit.)
Rotation optique 
[α] 20 D = -30 à -22 ° (C = 1 dans le toluène)
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

Methyl (S)-(-)-N-Z-aziridine-2-carboxylate is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a versatile building block in the synthesis of various pharmaceuticals and agrochemicals, allowing researchers to create complex molecular structures efficiently.
  • Chiral Auxiliary in Asymmetric Synthesis: Its chiral nature makes it an excellent choice for asymmetric synthesis, helping chemists produce enantiomerically pure compounds, which are crucial in drug development.
  • Bioconjugation Techniques: The compound can be employed in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their effectiveness in targeted therapies.
  • Material Science: It finds applications in the development of new materials, particularly in creating polymers with specific properties, which can be tailored for use in coatings or adhesives.
  • Research in Medicinal Chemistry: This compound is instrumental in the exploration of new therapeutic agents, particularly in the development of novel treatments for various diseases, due to its unique chemical properties.

Citations