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Atomfair 6,3-Glucuronolactone acetonide C9H12O6

Description 6,3-Glucuronolactone acetonide (CAS No. 20513-98-8) is a high-purity, specialized chemical compound with the molecular formula C9H12O6. Its IUPAC name, 9-hydroxy-4,4-dimethyl-3,5,7,11-tetraoxatricyclo[6.3.0.02,6]undecan-10-one , reflects its complex cyclic structure, which features multiple oxygen-containing functional groups. This compound is derived from D-glucuronolactone and is protected as an acetonide, enhancing its stability for synthetic applications. Ideal for researchers in carbohydrate chemistry, organic synthesis, and pharmaceutical development, our product is rigorously tested to ensure ??95% purity (HPLC). Available in quantities from milligrams to kilograms, it is supplied in amber glass vials or sealed containers to maintain integrity. Store in a cool, dry place under inert…

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Description

Description

6,3-Glucuronolactone acetonide (CAS No. 20513-98-8) is a high-purity, specialized chemical compound with the molecular formula C9H12O6. Its IUPAC name, 9-hydroxy-4,4-dimethyl-3,5,7,11-tetraoxatricyclo[6.3.0.02,6]undecan-10-one, reflects its complex cyclic structure, which features multiple oxygen-containing functional groups. This compound is derived from D-glucuronolactone and is protected as an acetonide, enhancing its stability for synthetic applications. Ideal for researchers in carbohydrate chemistry, organic synthesis, and pharmaceutical development, our product is rigorously tested to ensure ??95% purity (HPLC). Available in quantities from milligrams to kilograms, it is supplied in amber glass vials or sealed containers to maintain integrity. Store in a cool, dry place under inert conditions for optimal shelf life.

  • CAS No: 20513-98-8
  • Molecular Formula: C9H12O6
  • Molecular Weight: 216.19
  • Exact Mass: 216.06338810
  • Monoisotopic Mass: 216.06338810
  • IUPAC Name: 9-hydroxy-4,4-dimethyl-3,5,7,11-tetraoxatricyclo[6.3.0.02,6]undecan-10-one
  • SMILES: CC1(OC2C3C(C(C(=O)O3)O)OC2O1)C
  • Synonyms: 20513-98-8, 6,3-Glucuronolactone acetonide, D-Glucurono-6,3-lactone acetonide, 886749-48-0, 6-Hydroxy-2,2-dimethyltetrahydrofuro[2′,3′:4,5]furo[2,3-d][1,3]dioxol-5(3aH)-one

Application

6,3-Glucuronolactone acetonide serves as a key intermediate in the synthesis of modified sugars and glycosides, particularly in drug discovery and prodrug design. Its acetonide protection group allows selective manipulation of hydroxyl groups in complex carbohydrate frameworks. Researchers also utilize it in metabolic studies related to glucuronic acid pathways. The compound’s stability makes it suitable for multi-step organic transformations.

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