(2R,3R,4S,5S,6S)-2-(Acetoxymethyl)-6-hydroxytetrahydro-2H-pyran-3,4,5-triyl triacetate

97%

  • Product Code: 36482
  CAS:    22860-22-6
Molecular Weight: 348.30 g./mol Molecular Formula: C₁₄H₂₀O₁₀
EC Number: MDL Number: MFCD08274522
Melting Point: Boiling Point: 425.0±45.0°C at 760 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in carbohydrate chemistry research. It serves as a key intermediate in the preparation of glycosides, which are important for studying biological processes such as cell signaling and immune response. Additionally, it is used in the development of glycopeptides and glycoproteins, which have applications in drug discovery and vaccine development. Its acetylated structure allows for selective deprotection, enabling precise control over glycosylation reactions. This compound is also employed in the production of oligosaccharides, which are essential for understanding carbohydrate-protein interactions and designing therapeutic agents targeting these interactions.
Product Specification:
Test Specification
APPEARANCE White to light-yellow Solid
PURITY 96.5
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,660.00
+
-
0.250 10-20 days ฿3,520.00
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-
1.000 10-20 days ฿10,880.00
+
-
(2R,3R,4S,5S,6S)-2-(Acetoxymethyl)-6-hydroxytetrahydro-2H-pyran-3,4,5-triyl triacetate
This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in carbohydrate chemistry research. It serves as a key intermediate in the preparation of glycosides, which are important for studying biological processes such as cell signaling and immune response. Additionally, it is used in the development of glycopeptides and glycoproteins, which have applications in drug discovery and vaccine development. Its acetylated structure allows for selective deprotection, enabling precise control over glycosylation reactions. This compound is also employed in the production of oligosaccharides, which are essential for understanding carbohydrate-protein interactions and designing therapeutic agents targeting these interactions.
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