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Catalog Number:
41609
CAS Number:
87269-87-2
Chlorhydrate de benzyl ( S , S , S )-2-azabicyclo[3.3.0]octane-3-carboxylate
Purity:
96 - 101 % (dosage par titrage)
Synonym(s):
Chlorhydrate d'ester benzylique de l'acide ( S , S , S )-2-azabicyclo-[3,3,0]-octanecarboxylique, Chlorhydrate d'ester benzylique de l'acide ( S , S , S )-2-azabicyclo[3,3,0]octane-3-carboxylique
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Taille
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Informations sur le produit

Benzyl (S,S,S)-2-azabicyclo[3.3.0]octane-3-carboxylate hydrochloride is a versatile compound with significant applications in pharmaceutical research and development. This compound, also known as benzyl 2-azabicyclo[3.3.0]octane-3-carboxylate hydrochloride, exhibits unique structural properties that make it an attractive candidate for the synthesis of novel therapeutic agents. Its bicyclic structure contributes to its potential as a building block in drug discovery, particularly in the development of analgesics and other central nervous system-active compounds.

Researchers have found that this compound can serve as a key intermediate in the synthesis of various biologically active molecules, enhancing its relevance in medicinal chemistry. Its hydrochloride form improves solubility, making it easier to formulate in pharmaceutical applications. Additionally, the compound's stability and compatibility with various reaction conditions allow for its use in diverse synthetic pathways, providing a reliable option for chemists seeking to innovate in drug formulation and development.

Numéro CAS 
87269-87-2
Formule moléculaire
C15H19NO2 · HCl
Poids moléculaire 
281.78
Point de fusion 
176 - 180 °C (lit.)
Rotation optique 
[ á]20/D = -26° (C = 1 dans DMSO)
Informations générales
Numéro CAS 
87269-87-2
Formule moléculaire
C15H19NO2 · HCl
Poids moléculaire 
281.78
Point de fusion 
176 - 180 °C (lit.)
Rotation optique 
[ á]20/D = -26° (C = 1 dans DMSO)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Benzyl (S,S,S)-2-azabicyclo[3.3.0]octane-3-carboxylate hydrochloride 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 analgesics and anesthetics, enhancing pain management therapies.
  • Neuroscience Research: It is used in studies exploring neurotransmitter systems, particularly in the context of developing treatments for neurological disorders, providing insights into brain function and potential therapeutic targets.
  • Organic Synthesis: The compound acts as a versatile building block in organic chemistry, facilitating the creation of complex molecules, which is essential for researchers aiming to innovate in material science and drug discovery.
  • Biochemical Assays: It is employed in various biochemical assays to evaluate enzyme activity and metabolic pathways, helping researchers understand cellular processes and disease mechanisms.
  • Custom Synthesis Services: Many companies offer custom synthesis of this compound for specific research needs, allowing for tailored applications in academic and industrial laboratories, thus meeting diverse research requirements.

Citations