T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate CAS: 124655-09-0
Catalog Number | XD93413 |
Product Name | T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate |
CAS | 124655-09-0 |
Molecular Formula | C13H24O5 |
Molecular Weight | 260.33 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
T-Butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate is a chemical compound with a complex structure that is commonly used in organic synthesis and as a protective group in carbohydrate chemistry. It is known for its ability to efficiently protect hydroxyl groups and prevent unwanted reactions during various chemical transformations.One of the primary uses of T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate is in the synthesis of complex organic compounds. Hydroxyl groups are highly reactive and can undergo unwanted side reactions during chemical transformations. By selectively protecting these groups with the T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate moiety, chemists can control the reactions and obtain desired products. After the desired chemical transformations are complete, the protective group can be easily removed, allowing for the recovery of the original hydroxyl groups.In carbohydrate chemistry, T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate is commonly used for the protection of sugar molecules. Sugars contain multiple hydroxyl groups that can react with reagents, leading to undesired by-products. By selectively protecting these hydroxyl groups with T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate, chemists can manipulate the remaining hydroxyl groups without interference. This allows for the synthesis of complex sugar derivatives and the study of carbohydrate-protein interactions or the synthesis of glycoconjugates.Moreover, the T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate protective group is often used during the synthesis of natural products, pharmaceuticals, and other biologically active compounds. Its efficient protection and deprotection properties enable chemists to access a wide range of structurally diverse molecules. The protection of specific hydroxyl groups helps in controlling the reaction pathways and achieving the desired regioselectivity or stereoselectivity.In conclusion, T-butyl-(3R,5S)-6-hydroxy 3,5-O-isopropylidene 3,5-dihydroxyhexanoate is a versatile compound widely used in organic synthetic chemistry, particularly in the protection and deprotection of hydroxyl groups. Its unique structure allows for selective protection, enabling chemists to control reactions and obtain desired products. Its applications range from the synthesis of complex organic compounds to carbohydrate chemistry and the production of natural products and pharmaceuticals. The compound's ability to protect hydroxyl groups efficiently makes it an invaluable tool in various aspects of chemical research and development.