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Methyl 2,4,6-tri-O-acetyl-3-O-

(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-galactopyranoside
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  • wytsci
  • WT-CB-D40798
  • 2025年07月10日
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    • 英文名

      Methyl 2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-galactopyranoside

    • CAS号

      145251-15-6

    WT-CB-D40798
    Methyl 2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-galactopyranoside
    145251-15-6
    纯度:≥98%[1H-NMR]
    分子式:C27H38O18
    分子量:650.58
    储存:Store at 0 to 8 °C.
    性状:White Crystalline Solid
    溶剂:DCM, DMF, DMSO, EtOAc, MeOH
    别名:Methyl 3-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-galactopyranoside triacetate

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    Methyl 2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-galactopyranoside
    相关实验
    • Synthesis of 2-O-Alkyloligoribonucleotides

      2′-O -Alkyloligoribonucleotides possess properties that render them ideally suited for studying RNA processing and for the affinity chromatography of RNA-protein complexes. Particularly useful compounds are those in which alkyl is methyl (1 –

    • Optimizing Splice-Switching Oligomer Sequences Using 2-O-Methyl Phosphorothioate Chemistry

      and then a set of oligomers complementary to the acceptor and donor splice sites, as well as intra-exonic regions predicted to contain exon splice enhancers, are designed and synthesized as 2′-O-methyl-modified bases on a phosphorothioate backbone (2OMeAOs

    • Chemical Synthesis of 2-O-Alkylated siRNAs

      available 2�-O-methyl ribosides, 2′-alkyl groups bearing positive charges are especially promising candidates. We have shown that in a proper formulation they are superior to unmodified siRNAs. This may be due to enhanced stability and most probably

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    Methyl 2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-galactopyranoside
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