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

Catalog Number:
41418
CAS Number:
69257-04-1
Chlorure de N- benzylcinchonidinium
Purity:
≥ 98 % (HPLC)
Synonym(s):
(8 S ,9 R -(-)- N -Chlorure de benzylcinchonidinium, BCDC
Documents
$176.26 /10G
Taille
Request Bulk Quote
Informations sur le produit

N-Benzylcinchonidinium chloride is a versatile compound recognized for its unique properties and applications in various fields. This quaternary ammonium salt is primarily utilized in asymmetric synthesis and as a chiral auxiliary in organic chemistry, enabling researchers to achieve high enantioselectivity in reactions. Its ability to facilitate the formation of chiral centers makes it invaluable in the pharmaceutical industry, particularly in the development of new drugs where stereochemistry plays a crucial role.

Moreover, N-Benzylcinchonidinium chloride has shown promise in the field of catalysis, where it can enhance reaction rates and selectivity. Its effectiveness in promoting reactions under mild conditions makes it an attractive choice for chemists looking to optimize their processes. With its favorable properties, this compound stands out as a reliable tool for researchers and industry professionals aiming to innovate and improve their methodologies.

Numéro CAS 
69257-04-1
Formule moléculaire
C26H29ClN2O
Poids moléculaire 
420.98
Point de fusion 
210 °C (lit.)
Rotation optique 
[α] 20 D = -188 à -182 ° (C = 1 dans H 2 O)
Informations générales
Numéro CAS 
69257-04-1
Formule moléculaire
C26H29ClN2O
Poids moléculaire 
420.98
Point de fusion 
210 °C (lit.)
Rotation optique 
[α] 20 D = -188 à -182 ° (C = 1 dans H 2 O)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

N-Benzylcinchonidinium chloride is widely utilized in research focused on:

  • Chiral Separation: This compound is effective in chiral chromatography, helping researchers separate enantiomers in pharmaceuticals, which is crucial for drug efficacy and safety.
  • Asymmetric Synthesis: It plays a significant role in asymmetric synthesis, allowing chemists to create specific chiral compounds that are essential in the development of new drugs.
  • Biological Studies: The compound is used in biological research to study its effects on ion channels and receptors, providing insights into potential therapeutic targets.
  • Analytical Chemistry: It serves as a chiral auxiliary in various analytical techniques, enhancing the accuracy of stereochemical analysis in complex mixtures.
  • Pharmaceutical Development: Its unique properties make it valuable in the formulation of new medications, particularly in improving the solubility and bioavailability of active pharmaceutical ingredients.

Citations