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CAS 145124-97-6

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Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside

Description:
Ethyl 2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside is a glycoside derivative of rhamnose, characterized by the presence of a thioether functional group and an isopropylidene protecting group. This compound features a rhamnopyranoside structure, which is a six-membered sugar ring, and is known for its potential applications in organic synthesis and as a building block in carbohydrate chemistry. The thioether linkage imparts unique reactivity and stability compared to typical ether or ester linkages. The isopropylidene group serves as a protective group, enhancing the compound's stability under various reaction conditions. Ethyl 2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside is typically utilized in the synthesis of more complex carbohydrates and can be involved in various biochemical applications, including studies related to glycosylation reactions. Its specific properties, such as solubility and reactivity, can vary based on the solvent and conditions used in experiments.
Formula:C11H20O4S
Synonyms:
  • Ethyl 2,3-O-isopropylidene-alpha-L-thiorhamnopyranoside
  • Ethyl 2,3-O-isopropylidene-1-thio-α-L-rhaMnopyranoside
  • Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside
  • Ethyl-2,3-O-isopropylidene-a-L-thiorhamnopyranoside
  • α-D-Mannopyranoside, ethyl 6-deoxy-2,3-O-(1-methylethylidene)-1-thio-
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Found 2 products.
  • Ethyl-2,3-O-isopropylidene-a-L-thiorhamnopyranoside
    Glentham
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    Ethyl-2,3-O-isopropylidene-a-L-thiorhamnopyranoside

    CAS:

    Ref: 7W-GC4341

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  • Ethyl 2,3-O-isopropylidene-a-L-thiorhamnopyranoside
    Biosynth
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    Ethyl 2,3-O-isopropylidene-a-L-thiorhamnopyranoside

    CAS:
    <p>Ethyl 2,3-O-isopropylidene-a-L-thiorhamnopyranoside (Ip) is a glycosylation inhibitor that inhibits the formation of an alpha-(1,2)-link between glucose and mannose in the glycosylation of the pentasaccharide. The maximum tolerated dosages of Ip have been determined in HL-60 cells. Trichloroacetimidate is used as a substitute for Ip in these experiments because it can be dissolved in water and has a high therapeutic index. Convergent synthesis of Ip was achieved by reacting pentasaccharides with trichloroacetimidate to produce pentasaccharides with substituted mannose residues at position two and three.</p>
    Formula:C11H20O4S
    Purity:Min. 95%
    Molecular weight:248.34 g/mol

    Ref: 3D-ME08334

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