Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
41505
CAS Number:
183903-99-3
( S )-(+)- N -(Boc)-2-méthylpipéridine
Purity:
≥ 97,5 % (CG)
Synonym(s):
( S )-(+)- N - tert -(butoxycarbonyl)-2-méthylpipéridine
Documents
$165.65 /1G
Taille
Request Bulk Quote
Informations sur le produit

(S)-(+)-N-(Boc)-2-methylpiperidine is a versatile chemical compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This compound features a tert-butyl carbamate protecting group, which enhances its stability and reactivity, making it an essential intermediate in organic synthesis. Researchers and industry professionals appreciate its role in the development of chiral compounds, particularly in the pharmaceutical sector, where it serves as a building block for the synthesis of biologically active molecules. Its unique structure allows for selective reactions, facilitating the creation of complex molecules with high efficiency.

In addition to its applications in drug development, (S)-(+)-N-(Boc)-2-methylpiperidine is also valuable in the field of materials science, where it can be used to modify polymer properties. Its ability to act as a chiral auxiliary further expands its utility in asymmetric synthesis, providing researchers with a reliable tool for producing enantiomerically pure compounds. The compound's favorable characteristics, such as its ease of handling and compatibility with various reaction conditions, make it a preferred choice for professionals seeking to streamline their synthetic processes.

Numéro CAS 
183903-99-3
Formule moléculaire
C 11 H 21 NO 2
Poids moléculaire 
199.29
Indice de réfraction 
n20D 1.45 (Lit.)
Rotation optique 
[ á]20/D = 46 ° (C = 1 dans le chloroforme)
Informations générales
Numéro CAS 
183903-99-3
Formule moléculaire
C 11 H 21 NO 2
Poids moléculaire 
199.29
Indice de réfraction 
n20D 1.45 (Lit.)
Rotation optique 
[ á]20/D = 46 ° (C = 1 dans le chloroforme)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(S)-(+)-N-(Boc)-2-methylpiperidine is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a key building block in the synthesis of various pharmaceuticals, allowing chemists to create complex molecules efficiently.
  • Drug Development: Its unique structure makes it valuable in developing new drugs, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Chiral Catalysis: The chiral nature of this compound enables its use in asymmetric synthesis, which is crucial for producing enantiomerically pure substances, reducing the need for further purification steps.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter systems, helping researchers understand the mechanisms of action for various neuroactive compounds.
  • Material Science: The compound can be incorporated into polymers and materials, enhancing their properties for applications in coatings, adhesives, and other industrial products.

Citations