2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine
99%
- Product Code: 98137
Alias:
Tetra-O-pivaloyl-β-D-galactosamine
CAS:
108342-87-6
| Molecular Weight: | 515.64 g./mol | Molecular Formula: | C₂₆H₄₅NO₉ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00153054 | |
| Melting Point: | 92-95 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis as a protected form of galactosamine, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. Its pivaloyl groups provide stability during chemical reactions, making it suitable for glycosylation processes. It is also employed in the development of glycosidase inhibitors and in the study of carbohydrate-protein interactions. Additionally, it finds application in the synthesis of bioactive molecules, including potential drug candidates for treating bacterial infections and cancer. Its role in glycobiology research is significant, aiding in the exploration of cell signaling and immune response mechanisms.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 92 95? |
| Purity | 99 100% |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
| INFRARED SPECTROMETRY | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿10,570.00 |
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2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine
Used primarily in organic synthesis as a protected form of galactosamine, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. Its pivaloyl groups provide stability during chemical reactions, making it suitable for glycosylation processes. It is also employed in the development of glycosidase inhibitors and in the study of carbohydrate-protein interactions. Additionally, it finds application in the synthesis of bioactive molecules, including potential drug candidates for treating bacterial infections and cancer. Its role in glycobiology research is significant, aiding in the exploration of cell signaling and immune response mechanisms.
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