(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate
98%
- Product Code: 229171
CAS:
13992-16-0
Molecular Weight: | 440.46 g./mol | Molecular Formula: | C₂₀H₂₄O₉S |
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EC Number: | MDL Number: | ||
Melting Point: | 85-87 °C | Boiling Point: | 514.6±50.0 °C(Predicted) |
Density: | 1.31±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily as an intermediate in organic synthesis, especially in the preparation of glycosylation reagents and carbohydrate-based compounds. Its protected sugar structure with a phenylthio group makes it valuable in the construction of complex oligosaccharides and glycoconjugates, which are important in pharmaceutical research, particularly in vaccine development and drug design targeting infectious diseases and cancer. The acetate groups allow for selective deprotection, enabling stepwise assembly of sugar chains. Commonly employed in stereoselective synthesis due to its defined chiral centers.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.250 G | 10-20 days | ฿4,390.00 |
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1.000 G | 10-20 days | ฿9,890.00 |
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5.000 G | 10-20 days | ฿39,590.00 |
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(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate
Used primarily as an intermediate in organic synthesis, especially in the preparation of glycosylation reagents and carbohydrate-based compounds. Its protected sugar structure with a phenylthio group makes it valuable in the construction of complex oligosaccharides and glycoconjugates, which are important in pharmaceutical research, particularly in vaccine development and drug design targeting infectious diseases and cancer. The acetate groups allow for selective deprotection, enabling stepwise assembly of sugar chains. Commonly employed in stereoselective synthesis due to its defined chiral centers.
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