2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid monohydrate

CAS: 68539-16-2

Ref. 3D-MD13685

Produktinformation

• Name: 2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid monohydrate
• Synonyme: 2,3:4,6-Di-O-isopropylidene-2-C-hydroxy-L-gulonic acid2,3:4,6-Di-O-isopropylidene-a-L-xylo-2-hexulofuranosonic acid, (-)-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
• CAS: 68539-16-2

Beschreibung

2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid monohydrate is a natural product that is produced in a bioreactor by the reaction of sorbose and lipase. It can be used as a precursor to industrial chemicals, such as epoxides and ethers. The synthetic pathway for 2,3:4,6-di-O-isopropylidene-2-keto-l gulonic acid monohydrate (DIG) starts with the condensation of glycerol with sorbose in the presence of an enzyme such as lipase. The resulting intermediate is then oxidized to form 2,3:4,6 dihydroxyacetone phosphate (DHAP). DHAP reacts with hydrogen peroxide to form the corresponding ketone. This ketone can then react with hydrochloric acid to form 2,3:4,6 dihydroxy

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 292.28 g/mol
• Formel: C₁₂H₁₈O₇·H₂O
• Reinheit: Min. 95%
• Farbe/Form: White Powder