(1S,2S)-1-((2R,3R,4S,6S)-3-Acetamido-4-Acetoxy-6-((1-Acetyl-5-Bromo-4-Chloro-1H-Indol-3-Yl)Oxy)-6-(Methoxycarbonyl)Tetrahydro-2H-Pyran-2-Yl)Propane-1,2,3-Triyl Triacetate
98%
- Product Code: 237369
CAS:
153248-53-4
| Molecular Weight: | 761.95 g./mol | Molecular Formula: | C₃₀H₃₄BrClN₂O₁₄ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used in the synthesis of complex glycoconjugates and bioactive molecules, this compound serves as a key intermediate in pharmaceutical research, particularly in the development of antibiotic and antiviral agents. Its structural complexity allows for selective modifications in carbohydrate-based drug design. The presence of multiple acetyl and acetoxy groups enables controlled deprotection strategies, facilitating stepwise assembly of oligosaccharides. Additionally, the bromo and chloro substituents on the indole ring provide sites for cross-coupling reactions, making it valuable in medicinal chemistry for generating diverse compound libraries. It is also employed in studies involving enzyme inhibition and cell surface receptor targeting due to its mimicry of glycosylated natural substrates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿78,390.00 |
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(1S,2S)-1-((2R,3R,4S,6S)-3-Acetamido-4-Acetoxy-6-((1-Acetyl-5-Bromo-4-Chloro-1H-Indol-3-Yl)Oxy)-6-(Methoxycarbonyl)Tetrahydro-2H-Pyran-2-Yl)Propane-1,2,3-Triyl Triacetate
Used in the synthesis of complex glycoconjugates and bioactive molecules, this compound serves as a key intermediate in pharmaceutical research, particularly in the development of antibiotic and antiviral agents. Its structural complexity allows for selective modifications in carbohydrate-based drug design. The presence of multiple acetyl and acetoxy groups enables controlled deprotection strategies, facilitating stepwise assembly of oligosaccharides. Additionally, the bromo and chloro substituents on the indole ring provide sites for cross-coupling reactions, making it valuable in medicinal chemistry for generating diverse compound libraries. It is also employed in studies involving enzyme inhibition and cell surface receptor targeting due to its mimicry of glycosylated natural substrates.
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