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Catalog Number:
39601
CAS Number:
14347-83-2
( R )-4-Benciloximetil-2,2-dimetil-1,3-dioxolano
Purity:
≥ 97% (GC)
Documents
$212.32 /1G
Tamaño
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Información del producto

(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.

Número CAS
14347-83-2
Fórmula molecular
C13H18O3
Peso molecular
222.28
Número MDL
MFCD00066533
Densidad
1,05 g/ml
Índice de refracción
n20D = 1,49
Rotación óptica
[α]20 D = -18 a -21° (puro)
Condiciones
Tienda en RT
Información general
Número CAS
14347-83-2
Fórmula molecular
C13H18O3
Peso molecular
222.28
Número MDL
MFCD00066533
Densidad
1,05 g/ml
Índice de refracción
n20D = 1,49
Rotación óptica
[α]20 D = -18 a -21° (puro)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(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.

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