PI14053 1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose (CAS No.: 582-52-5)

1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose Description

1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose, with a defined molecular weight of 238.28 g/mol, is used as a protecting group in carbohydrate synthesis. The acetonide groups stabilise reactive hydroxyl sites during multi-step organic transformations. Its quantified purity ensures reproducibility in yields, making it suitable for iterative synthetic protocols in both research and industrial laboratory settings.

1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose Characteristics

*The above product information is based on theoretical data and is for reference only. Actual specifications may vary.

1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose Applications

Chemical Synthesis
- Used as a protecting group reagent in carbohydrate synthesis to minimise side reactions by temporarily masking hydroxyl groups, thereby enhancing selectivity in complex organic transformations.

Pharmaceutical Research
- Applied in the synthesis of intermediates for active pharmaceutical ingredients to control reactive functionalities. Its acetonide structure assists in achieving high reaction specificity and improved yield consistency.

Academic Research
- Employed in methodological studies to evaluate reaction mechanisms. The compound's defined molecular properties facilitate reproducible experimental conditions and help elucidate synthetic pathways.

1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose Packing

The product is packaged in moisture-resistant, sealed vials and placed within secondary protective cartons to minimise physical damage and contamination. The packaging material provides an effective barrier against environmental moisture. Storage recommendations call for a cool, dry location. Custom packaging solutions, including labelling and compartmentalisation, are available to address specific laboratory and shipping requirements.

Additional Information

Protecting group chemistry is a critical aspect of modern organic synthesis. Compounds like 1,2:5,6-Di-O-isopropylidene-α-D-glucofuranose play an essential role in the selective protection of functional groups during multistep reactions. Such reagents allow chemists to manage reactivity and improve the overall efficiency of synthetic protocols.

Furthermore, understanding the structural implications of acetonide formation assists researchers in optimising reaction conditions and yields. This compound's well-defined properties facilitate reproducibility in experiments, providing a reliable basis for both academic investigation and process development in industrial laboratories.