β-D-Ribofuranose 1-acetate 2,3,5-tribenzoate
98%
- Product Code: 58049
Alias:
1-Acetyl-2,3,5-tribenzoyloxy-1-beta-D-ribofuranose
CAS:
6974-32-9
Molecular Weight: | 504.48 g./mol | Molecular Formula: | C₂₈H₂₄O₉ |
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EC Number: | 230-220-4 | MDL Number: | MFCD00005357 |
Melting Point: | 128-130 °C | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used in the synthesis of nucleosides and nucleotides, which are essential for creating antiviral and anticancer drugs. Acts as a protected intermediate in organic chemistry, enabling selective reactions without affecting other functional groups. Applied in carbohydrate chemistry for modifying sugar molecules to study biological processes or develop new pharmaceuticals. Also utilized in the preparation of glycosyl donors for oligosaccharide synthesis, aiding in the development of glycoconjugate vaccines and other therapeutic agents. Its benzoate groups provide stability during chemical transformations, making it valuable in complex organic synthesis.
Product Specification:
Test | Specification |
---|---|
HEAVY METALS AS PB | 0ppm 10ppm |
Melting point | 127 130? |
PurityGC | 98 100% |
SPECIFIC ROTATION A20DC1 PYRIDINE | 23.9-24.9 |
WATER BY KARL FISCHER | 0 1% |
APPEARANCE | WHITE POWDER OR CRYSTALS |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿260.00 |
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5.000 | 10-20 days | ฿290.00 |
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25.000 | 10-20 days | ฿720.00 |
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100.000 | 10-20 days | ฿2,180.00 |
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500.000 | 10-20 days | ฿9,100.00 |
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β-D-Ribofuranose 1-acetate 2,3,5-tribenzoate
Used in the synthesis of nucleosides and nucleotides, which are essential for creating antiviral and anticancer drugs. Acts as a protected intermediate in organic chemistry, enabling selective reactions without affecting other functional groups. Applied in carbohydrate chemistry for modifying sugar molecules to study biological processes or develop new pharmaceuticals. Also utilized in the preparation of glycosyl donors for oligosaccharide synthesis, aiding in the development of glycoconjugate vaccines and other therapeutic agents. Its benzoate groups provide stability during chemical transformations, making it valuable in complex organic synthesis.
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