CAS 68539-16-2: 2,3:4,6-di-O-isopropylidene-2-keto-L-gulonic acid
Description:2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid is a chemical compound that belongs to the class of carbohydrates, specifically a derivative of L-gulonic acid. This compound features two isopropylidene protecting groups, which enhance its stability and solubility in organic solvents. The presence of the keto group at the second carbon position contributes to its reactivity and potential applications in organic synthesis. It is typically used in carbohydrate chemistry for the synthesis of various derivatives and intermediates. The compound is characterized by its ability to undergo various chemical transformations, making it a valuable building block in the synthesis of more complex molecules. Additionally, its structural features allow for specific interactions in biochemical applications, although it is not commonly found in nature. As with many organic compounds, proper handling and storage are essential to maintain its integrity and prevent degradation. Overall, 2,3:4,6-di-O-isopropylidene-2-keto-L-gulonic acid serves as an important tool in synthetic organic chemistry.
Formula:C12H20O8
InChI:InChI=1/C12H18O7.H2O/c1-10(2)15-5-6-7(17-10)8-12(16-6,9(13)14)19-11(3,4)18-8;/h6-8H,5H2,1-4H3,(H,13,14);1H2/t6-,7+,8-,12+;/m0./s1
- Synonyms:
- (-)-2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic Acid Monohydrate
- Diisoproyplideneketogulonicacidmonohydrate
- (-)-2,3:4,6-Di-O-isoproyplidene-2-keto-L-gulonic acid monohydrate
- Dikegulac acid
- (3aS,3bR,7aS,8aR)-2,2,5,5-tetramethyltetrahydro-8aH-[1,3]dioxolo[4,5]furo[3,2-d][1,3]dioxine-8a-carboxylic acid hydrate (non-preferred name)
- (-)-Diacetone-2-keto-L-gulonic acid monohydrate
