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Atomfair alpha-D-Glucofuranose, 1,2-O-(1-methylethylidene)- C9H16O6

Description ??-D-Glucofuranose, 1,2-O-(1-methylethylidene)- (CAS No. 18549-40-1) is a high-purity carbohydrate derivative with the molecular formula C9H16O6. This compound features a protected glucofuranose structure, where the 1,2-hydroxyl groups are shielded by an isopropylidene group, enhancing its stability for synthetic applications. Its IUPAC name, (1R)-1-[(3aR,5R,6S,6aR)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol, reflects its stereochemical complexity, making it valuable for chiral synthesis and glycosylation studies. Ideal for researchers in organic chemistry, glycobiology, and pharmaceutical development, this product is rigorously tested for purity and consistency. Available in various quantities to suit lab-scale and industrial needs.

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Description

Description

??-D-Glucofuranose, 1,2-O-(1-methylethylidene)- (CAS No. 18549-40-1) is a high-purity carbohydrate derivative with the molecular formula C9H16O6. This compound features a protected glucofuranose structure, where the 1,2-hydroxyl groups are shielded by an isopropylidene group, enhancing its stability for synthetic applications. Its IUPAC name, (1R)-1-[(3aR,5R,6S,6aR)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol, reflects its stereochemical complexity, making it valuable for chiral synthesis and glycosylation studies. Ideal for researchers in organic chemistry, glycobiology, and pharmaceutical development, this product is rigorously tested for purity and consistency. Available in various quantities to suit lab-scale and industrial needs.

  • CAS No: 18549-40-1
  • Molecular Formula: C9H16O6
  • Molecular Weight: 220.22
  • Exact Mass: 220.09468823
  • Monoisotopic Mass: 220.09468823
  • IUPAC Name: (1R)-1-[(3aR,5R,6S,6aR)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol
  • SMILES: CC1(O[C@@H]2[C@H]([C@H](O[C@@H]2O1)[C@@H](CO)O)O)C
  • Synonyms: 18549-40-1, NSC 1697, EINECS 242-420-9, .alpha.-D-Glucofuranose, 1,2-O-(1-methylethylidene)-, DTXSID80885054

Application

This compound serves as a key intermediate in the synthesis of modified sugars and nucleosides, particularly in carbohydrate chemistry research. It is used to study glycosylation reactions and enzyme mechanisms due to its protected hydroxyl groups. Researchers also employ it in the development of prodrugs and targeted therapeutics requiring stable sugar moieties.

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