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Catalog Number:
32381
CAS Number:
73346-74-4
-)-2,3- O -isopropiliden-D-treitol
Purity:
≥ 98% (GC)
Synonym(s):
( 4R , 5R- 2,2-Dimetil-1,3-dioxolano-4,5-dimetanol, (4 R ,5 R -(-)-4,5-Bis(hidroximetil)-2,2-dimetil-1,3-dioxolano
Documents
$43.87 /1G
Tamaño
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Información del producto

Conservar alejado de agentes oxidantes y fuentes de ignición. Conservar en atmósfera de gas inerte (por ejemplo, argón).

Número CAS
73346-74-4
Fórmula molecular
C7H14O4
Peso molecular
162.19
Número MDL
MFCD00009761
Punto de fusión
47-52° C
Punto de ebullición
88-90 °C / 0,05 mmHg
Rotación óptica
[a]20/D= -3 a -5° (C=5 en acetona)
Condiciones
Conservar a ≤ -10 °C
Información general
Número CAS
73346-74-4
Fórmula molecular
C7H14O4
Peso molecular
162.19
Número MDL
MFCD00009761
Punto de fusión
47-52° C
Punto de ebullición
88-90 °C / 0,05 mmHg
Rotación óptica
[a]20/D= -3 a -5° (C=5 en acetona)
Condiciones
Conservar a ≤ -10 °C
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(-)-2,3-O-Isopropylidene-D-threitol is widely utilized in research focused on:

  • Synthesis of Carbohydrate Derivatives: This compound serves as a key intermediate in the synthesis of various carbohydrate derivatives, which are essential in the development of pharmaceuticals and glycosylation reactions.
  • Protecting Group in Organic Chemistry: It acts as an effective protecting group for hydroxyl functionalities during multi-step organic synthesis, enhancing the yield and purity of final products.
  • Research in Glycobiology: The compound is valuable in glycobiology studies, aiding in the exploration of glycan structures and their biological functions, which can lead to advancements in drug development.
  • Development of Antiviral Agents: Its derivatives have shown potential in the formulation of antiviral agents, contributing to the fight against viral infections by modifying sugar moieties.
  • Biochemical Applications: Used in the preparation of various biochemical probes, it helps researchers study enzyme activities and interactions, providing insights into metabolic pathways.

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