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CAS 103674-69-7

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Bromo-2,3,4-tri-O-benzoyl-α-D-glucuronic Acid Methyl Ester

Description:
Bromo-2,3,4-tri-O-benzoyl-α-D-glucuronic Acid Methyl Ester is a complex organic compound characterized by its structural features, which include a glucuronic acid backbone modified with three benzoyl groups and a methyl ester functional group. This compound is typically used in organic synthesis and carbohydrate chemistry, particularly in the context of glycosylation reactions and the study of glycosides. The presence of the bromine atom suggests potential reactivity, making it useful in various chemical transformations. The benzoyl groups enhance the lipophilicity and stability of the molecule, while the methyl ester provides a protective group that can be selectively removed in further synthetic steps. Its solubility properties are influenced by the benzoyl substituents, allowing for its use in various organic solvents. As with many derivatives of sugars, it may exhibit specific biological activities, although detailed biological data would depend on experimental studies. Overall, this compound serves as a valuable intermediate in the synthesis of more complex carbohydrate-based molecules.
Formula:C28H23BrO9
InChI:InChI=1/C28H23BrO9/c1-34-28(33)23-21(37-26(31)18-13-7-3-8-14-18)20(36-25(30)17-11-5-2-6-12-17)22(24(29)35-23)38-27(32)19-15-9-4-10-16-19/h2-16,20-24H,1H3/t20-,21-,22-,23?,24-/m0/s1
SMILES:COC(=O)C1[C@H]([C@@H]([C@@H]([C@@H](Br)O1)OC(=O)c1ccccc1)OC(=O)c1ccccc1)OC(=O)c1ccccc1
Synonyms:
  • 1-Bromo-1-deoxy-2,3,4-tribenzoate α-D-Glucopyranuronic Acid Methyl Ester
  • Methyl (2,3,4-Tri-O-benzoyl-α-D-glucopyranosyl bromide)uronate
  • Bromo-2,3,4-tri-O-benzoyl-a-D-glucuronic Acid Methyl Ester
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