D-Glucurono-6,3-lactone acetonide
≥98%
- Product Code: 98004
Alias:
D-glucuronic acid-γ-lactone acetonide ;D-glucuronic acid-γ-lactone acetonide
CAS:
20513-98-8
| Molecular Weight: | 216.19 g./mol | Molecular Formula: | C₉H₁₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00061641 | |
| Melting Point: | 119-121°C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of various biologically active molecules, including glycosides and polysaccharides. Its acetonide group provides protection for specific hydroxyl groups during chemical reactions, enabling selective modifications and transformations. This feature is especially valuable in the synthesis of pharmaceutical agents and natural products, where precise control over molecular structure is crucial. Additionally, it finds application in the development of chiral building blocks for asymmetric synthesis, contributing to the creation of enantiomerically pure compounds used in drug discovery and development. Its role in carbohydrate chemistry also extends to the study of enzyme mechanisms and the design of enzyme inhibitors, aiding in the understanding of biochemical pathways and the development of therapeutic interventions.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 119 123? |
| PurityGC | 98 100% |
| SPECIFIC ROTATION A20DC1 WATER | 63.5-70.5 |
| APPEARANCE | WHITE POWDER OR CRYSTALS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿522.00 |
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| 25.000 | 10-20 days | ฿1,980.00 |
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D-Glucurono-6,3-lactone acetonide
This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of various biologically active molecules, including glycosides and polysaccharides. Its acetonide group provides protection for specific hydroxyl groups during chemical reactions, enabling selective modifications and transformations. This feature is especially valuable in the synthesis of pharmaceutical agents and natural products, where precise control over molecular structure is crucial. Additionally, it finds application in the development of chiral building blocks for asymmetric synthesis, contributing to the creation of enantiomerically pure compounds used in drug discovery and development. Its role in carbohydrate chemistry also extends to the study of enzyme mechanisms and the design of enzyme inhibitors, aiding in the understanding of biochemical pathways and the development of therapeutic interventions.
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