2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose
Product Name |
2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose
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Product Code |
T00002423
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Chemical name |
2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose
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Synonyms |
(2R,3S,4R,5R,6S)-2-(Acetoxymethyl)-6-(phenylthio)-5-(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)tetrahydro-2H-pyran-3,4-diyl Diacetate
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Impurity |
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CAS Number |
217814-68-1
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Alternate CAS # |
NA
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Molecular form |
C₂₆H₂₁Cl₄NO₉S
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Appearance |
Light Yellow Solid
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Melting Point |
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Mol. Weight |
665.32
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Storage |
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Solubility |
Ethyl Acetate, DCM
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Stability |
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Category |
Aromatics, Carbohydrates & Derivatives, Intermediates, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
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Boiling Point |
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Applications |
2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose is an intermediate formed in the synthesis of N-Acetylchitooctaose (A168460), a chitooligosaccharide used to activate Saccharomyces cerevisiae chitin biosynthesis. N-Acetylchitooctaose has affinity for NKR-P1A protein, the major activating receptor at the surface of rat natural killer (NK) cells, and may be useful in human therapy in cancer treatment (colon cancer, melanoma).
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Dangerous Goods Info |
NA
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References |
Becker, H.F. et al.: BMC Res. Notes, 4, 454 (2011); Kren, V. et al.: NATO, Sci. Ser. Math. Phys. Chem., 129, 379 (2003)
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Extra Notes |
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Documents (MSDS) |
No Data Available
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Keywords |
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