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Catalog Number:
39601
CAS Number:
14347-83-2
( R )-4-Benzyloxyméthyl-2,2-diméthyl-1,3-dioxolane
Purity:
≥ 97% (CG)
Documents
$212.32 /1G
Taille
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Informations sur le produit

(R)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane is a versatile compound widely utilized in organic synthesis and pharmaceutical development. This chiral dioxolane derivative is particularly valued for its ability to serve as a protecting group for alcohols and amines, facilitating complex reaction pathways while maintaining the integrity of sensitive functional groups. Its unique structure allows for selective reactions, making it an essential tool for chemists working on the synthesis of intricate molecules, including natural products and pharmaceuticals.

In addition to its role in synthesis, (R)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane is also explored for its potential applications in the development of novel drug candidates. Researchers appreciate its stability and reactivity, which can be tailored for specific applications in medicinal chemistry. The compound's favorable properties make it an attractive choice for those looking to streamline their synthetic processes while achieving high yields and purity in their final products.

Numéro CAS 
14347-83-2
Formule moléculaire
C13H18O3
Poids moléculaire 
222.28
Indice de réfraction 
n20D = 1,49
Rotation optique 
[α]20 D = -18 à -21 ° (pur)
Informations générales
Numéro CAS 
14347-83-2
Formule moléculaire
C13H18O3
Poids moléculaire 
222.28
Indice de réfraction 
n20D = 1,49
Rotation optique 
[α]20 D = -18 à -21 ° (pur)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(R)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane is widely utilized in research focused on

  • Synthesis of Pharmaceutical Compounds: This compound serves as a versatile intermediate in the synthesis of various pharmaceuticals, enhancing the efficiency of drug development processes.
  • Chiral Auxiliary in Asymmetric Synthesis: Its chiral nature makes it an excellent auxiliary for asymmetric synthesis, allowing researchers to produce enantiomerically pure compounds, which are crucial in medicinal chemistry.
  • Protecting Group in Organic Chemistry: It acts as a protecting group for alcohols during multi-step synthesis, facilitating the selective transformation of other functional groups without interference.
  • Material Science Applications: This chemical is explored in the development of novel materials, particularly in creating polymers with specific properties for use in coatings and adhesives.
  • Research in Green Chemistry: Its application in green chemistry initiatives is notable, as it contributes to more sustainable synthetic pathways by reducing waste and improving reaction conditions.

Citations