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Catalog Number:
39604
CAS Number:
125995-13-3
2-[(4 R ,6 R )-6-(2-aminoéthyl)-2,2-diméthyl-1,3-dioxan-4-yl]acétate de tert -butyle
Purity:
≥ 98% (CG)
Synonym(s):
Ester tert -butylique de l'acide 2-[(4 R ,6 R )-6-(2-aminoéthyl)-2,2-diméthyl-1,3-dioxan-4-yl]acétique
Documents
$33.75 /1G
Taille
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Informations sur le produit

tert-Butyl 2-[(4R,6R)-6-(2-aminoethyl)-2,2-dimethyl-1,3-dioxan-4-yl]acetate is a versatile compound with significant applications in the pharmaceutical and chemical industries. This compound is recognized for its unique structure, which includes a dioxane ring that enhances its stability and reactivity, making it an excellent candidate for drug formulation and development. Its aminoethyl group provides potential for further functionalization, allowing researchers to explore various derivatives that could lead to novel therapeutic agents.

In practical applications, tert-Butyl 2-[(4R,6R)-6-(2-aminoethyl)-2,2-dimethyl-1,3-dioxan-4-yl]acetate can be utilized in the synthesis of bioactive molecules, particularly in the development of targeted drug delivery systems. Its favorable properties, such as solubility and compatibility with various solvents, make it an ideal choice for researchers looking to enhance the efficacy of their formulations. Additionally, its stability under various conditions ensures reliable performance in laboratory settings, making it a valuable asset for both academic and industrial research.

Numéro CAS 
125995-13-3
Formule moléculaire
C 14 H 274
Poids moléculaire 
273.37
Indice de réfraction 
n20D = 1,45
Rotation optique 
[α]20 D = 13 - 16 ° (C=1 dans CHCl 3 )
Informations générales
Numéro CAS 
125995-13-3
Formule moléculaire
C 14 H 274
Poids moléculaire 
273.37
Indice de réfraction 
n20D = 1,45
Rotation optique 
[α]20 D = 13 - 16 ° (C=1 dans CHCl 3 )
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

tert-Butyl 2-[(4R,6R)-6-(2-aminoethyl)-2,2-dimethyl-1,3-dioxan-4-yl]acetate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and bioavailability.
  • Biochemical Research: It is used in studies involving enzyme inhibitors, helping researchers understand enzyme mechanisms and develop new therapeutic agents.
  • Cosmetic Formulations: The compound is incorporated into skincare products for its stabilizing properties, improving product shelf life and effectiveness.
  • Polymer Chemistry: It acts as a building block for creating advanced polymers, which are essential in developing materials with specific properties for industrial applications.
  • Analytical Chemistry: This chemical is utilized as a standard in chromatography, aiding in the accurate analysis of complex mixtures in various samples.

Citations