2,3,4-Tri-O-acetyl-a-D-glucuronide methyl ester trichloroacetimidate
98%
- Product Code: 66409
Alias:
3,4,6-tri-o-acetyl-ALPHA-D-glucopyranose 1,2-(methyl orthoate); 3,4,6-tri-oxo-acetyl-α-D-glucopyranose 1 ,2-(Methyl orthoacetate)
CAS:
92420-89-8
| Molecular Weight: | 478.66 g./mol | Molecular Formula: | C₁₅H₁₈Cl₃NO₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02094293 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, stored in inert gas |
Product Description:
This compound is primarily utilized in synthetic organic chemistry as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its trichloroacetimidate group makes it a highly reactive glycosyl donor, enabling efficient glycosylation reactions under mild conditions. This is particularly valuable in the synthesis of glycoconjugates, which are essential in the development of pharmaceuticals, vaccines, and biochemical probes. Additionally, its acetyl-protected glucuronide moiety allows for selective deprotection, facilitating the construction of diverse carbohydrate structures. This compound is also employed in the study of enzymatic processes and the development of glycosidase inhibitors, which have potential therapeutic applications in treating metabolic disorders and infections.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Powder |
| PURITY | 97.5-100 |
| COMPOSITION | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £70.79 |
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| 1.000 | 10-20 days | £210.11 |
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2,3,4-Tri-O-acetyl-a-D-glucuronide methyl ester trichloroacetimidate
This compound is primarily utilized in synthetic organic chemistry as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its trichloroacetimidate group makes it a highly reactive glycosyl donor, enabling efficient glycosylation reactions under mild conditions. This is particularly valuable in the synthesis of glycoconjugates, which are essential in the development of pharmaceuticals, vaccines, and biochemical probes. Additionally, its acetyl-protected glucuronide moiety allows for selective deprotection, facilitating the construction of diverse carbohydrate structures. This compound is also employed in the study of enzymatic processes and the development of glycosidase inhibitors, which have potential therapeutic applications in treating metabolic disorders and infections.
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