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CAS 23202-66-6

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α-D-Glucopyranosyl bromide, 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-, 2,4,6-triacetate

Description:
α-D-Glucopyranosyl bromide, 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-, 2,4,6-triacetate, with CAS number 23202-66-6, is a complex glycosylated compound characterized by its acetylated glucopyranosyl units. This compound features a bromide substituent, which enhances its reactivity, particularly in glycosylation reactions. The presence of multiple acetyl groups indicates that it is a derivative of glucose, which can influence its solubility and stability in various solvents. The acetylation also serves to protect hydroxyl groups, making the compound more suitable for further chemical modifications. Its structure suggests potential applications in carbohydrate chemistry, particularly in the synthesis of oligosaccharides or glycosides. Additionally, the compound may exhibit specific biological activities due to its glycosylated nature, which can affect interactions with biological macromolecules. Overall, this compound is of interest in both synthetic organic chemistry and potential pharmaceutical applications, owing to its unique structural features and reactivity.
Formula:C26H35BrO17
InChI:InChI=1S/C26H35BrO17/c1-10(28)35-8-17-19(37-12(3)30)21(23(25(27)42-17)40-15(6)33)44-26-24(41-16(7)34)22(39-14(5)32)20(38-13(4)31)18(43-26)9-36-11(2)29/h17-26H,8-9H2,1-7H3/t17-,18-,19-,20-,21+,22+,23-,24-,25+,26+/m1/s1
InChI key:InChIKey=OCVWJMGXJXJBCO-VRECAULFSA-N
SMILES:O([C@H]1[C@H](OC(C)=O)[C@@H](COC(C)=O)O[C@H](Br)[C@@H]1OC(C)=O)[C@H]2[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O2
Synonyms:
  • Glucopyranosyl bromide, 3-O-β-D-glucopyranosyl-, heptaacetate, α-D-
  • α-D-Glucopyranosyl bromide, 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-, 2,4,6-triacetate
  • Acetobromolaminaribiose
  • α-D-Glucopyranosyl bromide, 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-, triacetate
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