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Catalog Number:
41510
CAS Number:
194726-40-4
Éthyl ( R ) -N -Boc-pipéridine-3-carboxylate
Purity:
≥ 95%
Synonym(s):
Ester éthylique de l'acide ( R )-(-)- N -Boc-nipécotique, Ester éthylique de l'acide ( R )-1-( tert -butoxycarbonyl)-pipéridine-3-carboxylique, (R)-1-(tert-butyl) 3-éthyl 1,3-pipéridinedicarboxylate, (3R)-1-tert-butoxycarbonyl-3-pipéridinecarboxylate d'éthyle
Documents
$136.00 /1G
Taille
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Informations sur le produit

Ethyl (R)-N-Boc-piperidine-3-carboxylate is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound features a piperidine ring, which is known for its ability to serve as a building block in the development of various pharmaceuticals and agrochemicals. Its unique structure, characterized by the Boc (tert-butoxycarbonyl) protecting group, enhances its stability and reactivity, making it an ideal candidate for peptide synthesis and other complex organic reactions. Researchers appreciate its role in the synthesis of bioactive molecules, particularly in the development of novel therapeutics targeting neurological disorders.

The practical applications of Ethyl (R)-N-Boc-piperidine-3-carboxylate extend to the production of chiral intermediates, which are essential in the pharmaceutical industry for creating enantiomerically pure compounds. Its favorable properties, such as ease of handling and compatibility with various reaction conditions, make it a preferred choice for chemists looking to streamline their synthesis processes. Additionally, its potential for use in asymmetric synthesis highlights its importance in the creation of drugs with improved efficacy and reduced side effects, thereby enhancing patient outcomes.

Numéro CAS 
194726-40-4
Formule moléculaire
C 13 H 23 NON 4
Poids moléculaire 
257.33
Point de fusion 
36 - 40 °C
Informations générales
Numéro CAS 
194726-40-4
Formule moléculaire
C 13 H 23 NON 4
Poids moléculaire 
257.33
Point de fusion 
36 - 40 °C
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

Ethyl (R)-N-Boc-piperidine-3-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.
  • Drug Development: It is commonly used in the development of new drugs, particularly in creating piperidine derivatives that exhibit biological activity, making it valuable in medicinal chemistry.
  • Peptide Synthesis: The compound plays a crucial role in peptide synthesis, acting as a protecting group for amines, which helps in the selective modification of amino acids during the synthesis process.
  • Material Science: It is applied in the formulation of advanced materials, including polymers and coatings, where its unique properties enhance the performance and durability of the final products.
  • Research and Development: Ethyl (R)-N-Boc-piperidine-3-carboxylate is essential in academic and industrial research settings, facilitating the exploration of new chemical reactions and methodologies.

Citations