Application and Effect
The effect of 2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose is to provide protection to the hydroxyl groups on the mannose molecule. This compound forms a protective shield around the hydroxyl groups at positions 2, 3, 5, and 6, preventing unwanted reactions from occurring at those sites.The primary application of 2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose is in the field of carbohydrate chemistry and synthesis. Carbohydrates are crucial molecules involved in various biological processes such as cell-cell recognition, cell signaling, and immune response. By selectively protecting specific hydroxyl groups on the mannose molecule, chemists can control and modify other functional groups without affecting the protected hydroxyls.The compound finds utility in the synthesis of complex carbohydrates and glycoconjugates. Glycoconjugates are molecules that consist of a carbohydrate moiety attached to another molecule, such as a protein or lipid. These molecules play critical roles in biological systems, including cell adhesion, immune response, and pathogen recognition.By utilizing 2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose, researchers can introduce modifications to specific regions of the mannose molecule within a glycoconjugate, without interfering with the protected hydroxyl groups. This enables the synthesis of customized glycoconjugates for various applications, such as drug development, diagnostics, and vaccine design.In summary, the effect of 2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose is the protection of hydroxyl groups on the mannose molecule, and its application lies in the synthesis of complex carbohydrates and glycoconjugates with potential use in diverse fields of research and industry.Product Sample
Product Packing:
Additional Information:
| Composition | C12H20O6 |
| Assay | 99% |
| Appearance | White to off-white powder |
| CAS No. | 14131-84-1 |
| Packing | Small and bulk |
| Shelf Life | 2 years |
| Storage | Store in cool and dry area |
| Certification | ISO. |