M6633

α-D-Mannose pentaacetate

• Sinónimos: 1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose
• Fórmula empírica (notación de Hill): C₁₆H₂₂O₁₁
• Número CAS: 4163-65-9
• Peso molecular: 390.34
• NACRES: NA.25
• PubChem Substance ID: 24897100
• UNSPSC Code: 12352201
• MDL number: MFCD00069798

Propiedades

• biological source: plant (ivory nut palm)
• Quality Segment: 200
• assay: ≥98% (TLC)
• form: powder
• optical activity: [α]25/D 55.0 to 55.8°, c = 2.2% (w/v) in chloroform
• technique(s): thin layer chromatography (TLC): suitable
• solubility: chloroform: 100 mg/mL, clear, colorless
• storage temp.: −20°C
• SMILES string: CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
• InChI: 1S/C16H22O11/c1-7(17)22-6-12-13(23-8(2)18)14(24-9(3)19)15(25-10(4)20)16(27-12)26-11(5)21/h12-16H,6H2,1-5H3
• InChI key: LPTITAGPBXDDGR-UHFFFAOYSA-N

Descripción

General description

Mannose is a monosaccharide.

Application

α-D-Mannose pentaacetate was used for glycosylation in a study that assessed novel synthetic inhibitors of selectin-mediated cell adhesion. It has also been used in a study to investigate stereospecific entry to spiroketal glycosides using alkylidenecarbene C−H insertion.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Información de seguridad

• Clase de almacenamiento: 11 - Combustible Solids
• ¿Qué está pasando?: WGK 3
• Punto de inflamación (°F): Not applicable
• Punto de inflamación (°C): Not applicable
• EPI (equipos de protección individual): Eyeshields, Gloves, type N95 (US)