M6633

α-D-Mannose-pentaacetat

• Synonym(e): 1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose
• Empirische Formel (Hill-System): C₁₆H₂₂O₁₁
• CAS-Nummer: 4163-65-9
• Molekulargewicht: 390.34
• MDL-Nummer: MFCD00069798
• UNSPSC-Code: 12352201
• PubChem Substanz-ID: 24897100
• NACRES: NA.25

Eigenschaften

• Biologische Quelle: plant (ivory nut palm)
• Qualitätsniveau: 200
• Assay: ≥98% (TLC)
• Form: powder
• Optische Aktivität: [α]25/D 55.0 to 55.8°, c = 2.2% (w/v) in chloroform
• Methode(n): thin layer chromatography (TLC): suitable
• Löslichkeit: chloroform: 100 mg/mL, clear, colorless
• Lagertemp.: −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
• InChIKey: LPTITAGPBXDDGR-UHFFFAOYSA-N

Beschreibung

Allgemeine Beschreibung

Mannose is a monosaccharide.

Anwendung

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.

Sonstige Hinweise

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

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)