2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
98%
- Product Code: 93715
Alias:
2,3,4,6-Tetra-O-acetyl-β-D-glucopyranose isothiocyanate
CAS:
14152-97-7
| Molecular Weight: | 389.38 g./mol | Molecular Formula: | C₁₅H₁₉NO₉S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00043085 | |
| Melting Point: | 114-116 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily used in the synthesis of glycosyl derivatives, particularly in the preparation of thioglycosides, which are valuable intermediates in carbohydrate chemistry. It serves as a key reagent for the introduction of the isothiocyanate functional group into sugar molecules, enabling the creation of glycosyl thioureas and other glycosylated compounds. These derivatives are often employed in the development of bioactive molecules, including glycoconjugates, which have applications in drug discovery and biochemical research. Additionally, it is utilized in the study of enzyme inhibitors and the modification of natural products to enhance their biological activity or stability. Its role in glycosylation reactions makes it a valuable tool in organic synthesis and medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 113 117? |
| PURITYHPLC | 97.5 100% |
| APPEARANCE | White or off-white powder |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,260.00 |
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| 0.500 | 10-20 days | ฿11,780.00 |
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| 1.000 | 10-20 days | ฿21,680.00 |
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2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
This chemical is primarily used in the synthesis of glycosyl derivatives, particularly in the preparation of thioglycosides, which are valuable intermediates in carbohydrate chemistry. It serves as a key reagent for the introduction of the isothiocyanate functional group into sugar molecules, enabling the creation of glycosyl thioureas and other glycosylated compounds. These derivatives are often employed in the development of bioactive molecules, including glycoconjugates, which have applications in drug discovery and biochemical research. Additionally, it is utilized in the study of enzyme inhibitors and the modification of natural products to enhance their biological activity or stability. Its role in glycosylation reactions makes it a valuable tool in organic synthesis and medicinal chemistry.
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