2,3,4-Tri-O-acetyl-1,6-anhydro-b-D-glucopyranose

CAS: 13242-55-2

Ref. 3D-MT06721

Produktinformation

• Name: 2,3,4-Tri-O-acetyl-1,6-anhydro-b-D-glucopyranose
• Synonyme: 1,6-Anhydro-b-D-glucose triacetateLevoglucosan triacetate, (1R,2R,3S,4R,5R)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triyl triacetate (non-preferred name), (1S,2R,3S,4R,5S)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triyl triacetate (non-preferred name), 1,6-Anhydro-2,3,4-tri-O-acetyl--D-glucopyranose, 1,6-Anhydro-2,3,4-tri-O-acetyl-β-<span class="text-smallcaps">D</span>-glucopyranose, 1,6-Anhydro-β-<span class="text-smallcaps">D</span>-glucopyranose triacetate, 1,6-anhydro-B-D-glucose 2,3,4-*triacetate, 2,3,4-Tri-O-acetyl-1,6-anhydro-β-<span class="text-smallcaps">D</span>-glucopyranose, 6,8-Dioxabicyclo[3.2.1]Octane-2,3,4-Triyl Triacetate (Non-Preferred Name), 6,8-Dioxabicyclo[3.2.1]octane, β-<span class="text-smallcaps">D</span>-glucopyranose deriv., Levoglucosan, triacetate, NSC 25284, Triacetyllevoglucosan, β-<span class="text-smallcaps">D</span>-Glucopyranose, 1,6-anhydro-, 2,3,4-triacetate, β-<span class="text-smallcaps">D</span>-Glucopyranose, 1,6-anhydro-, triacetate, β-D-Glucopyranose, 1,6-anhydro-, triacetate, β-D-Glucopyranose, 1,6-anhydro-, 2,3,4-triacetate, 6,8-Dioxabicyclo[3.2.1]octane, β-D-glucopyranose deriv.

Beschreibung

2,3,4-Tri-O-acetyl-1,6-anhydro-b-D-glucopyranose is a high purity monosaccharide that is custom synthesized to meet your needs. This product is a sugar with a click modification, fluorination, glycosylation and methylation. It can be used as a synthetic oligosaccharide or monosaccharide in the synthesis of complex carbohydrates. It has CAS No. 13242-55-2 and can be used in saccharides.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 288.25 g/mol
• Formel: C₁₂H₁₆O₈
• Reinheit: Min. 95%
• Farbe/Form: White Powder
• InChl: InChI=1S/C12H16O8/c1-5(13)17-9-8-4-16-12(20-8)11(19-7(3)15)10(9)18-6(2)14/h8-12H,4H2,1-3H3/t8-,9-,10+,11-,12-/m1/s1
• InChI Key: InChIKey=BAKQMOSGYGQJOJ-RMPHRYRLSA-N
• SMILES: CC(=O)O[C@H]1[C@H](OC(C)=O)[C@H]2CO[C@H](O2)[C@@H]1OC(C)=O