Phenyl 4-O-acetyl-2,6-di-O-benzoyl-1-thio-β-thio-β-D-galactopyranoside
≥98%
- Product Code: 96954
CAS:
152488-28-3
| Molecular Weight: | 522.57 g./mol | Molecular Formula: | C₂₈H₂₆O₈S |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. Its structure, featuring protective groups like acetyl and benzoyl, makes it valuable for selective glycosylation reactions, enabling the construction of specific glycosidic bonds. It is particularly useful in the synthesis of oligosaccharides and glycoproteins, which are essential in biological studies and drug development. Additionally, it serves as a building block in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Its thio-glycoside moiety enhances its reactivity, making it a versatile tool in synthetic organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿4,995.00 |
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| 0.025 | 10-20 days | ฿17,415.00 |
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| 0.100 | 10-20 days | ฿55,611.00 |
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Phenyl 4-O-acetyl-2,6-di-O-benzoyl-1-thio-β-thio-β-D-galactopyranoside
This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. Its structure, featuring protective groups like acetyl and benzoyl, makes it valuable for selective glycosylation reactions, enabling the construction of specific glycosidic bonds. It is particularly useful in the synthesis of oligosaccharides and glycoproteins, which are essential in biological studies and drug development. Additionally, it serves as a building block in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Its thio-glycoside moiety enhances its reactivity, making it a versatile tool in synthetic organic chemistry.
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