117205-81-9

Usage

Uses

Used in Pharmaceutical Industry:
(S)-(-)-2, 2 DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLATE is used as an intermediate in the synthesis of methoxypropionamide derivatives, which possess anticonvulsant activities. These derivatives have potential applications in the development of medications for the treatment of epilepsy and other seizure disorders, offering an alternative to conventional anticonvulsant drugs.
As an intermediate, (S)-(-)-2, 2 DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLATE plays a crucial role in the chemical reactions that lead to the formation of the final pharmaceutical products. Its unique structure and properties enable the synthesis of a variety of methoxypropionamide derivatives with potential therapeutic benefits.

Upstream product

• 22323-80-4 (4S)-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 60456-21-5 methyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 
• 1707-77-3 1,2:5,6-di-O-isopropylidene-D-mannitol 
• 15042-01-0 5,6-O-isopropylidene-L-ascorbic acid 

Downstream Products

• 102045-96-5 2,3-O-isopropylidene-L-glyceric acid 
• 60456-21-5 methyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 
• 116561-26-3 (2S)-2,3-isopropylideneglyceryl chloride 
• 130437-03-5 (S)-2,2-Dimethyl-[1,3]dioxolane-4-carboxylic acid (3-amino-5-nitro-phenyl)-amide 
• 130436-98-5 C₁₈H₂₃N₃O₈ 
• 68981-29-3 C₁₈H₂₃N₃O₈ 
• 73945-73-0 O-Isopropyliden-D-glycerinsaeurechlorid 
• 97652-53-4 N-(O-Isopropyliden-D-glyceroyl)-L-phenylalanin 
• 97652-45-4 N-(O-Isopropyliden-D-glyceroyl)-L-phenylalaninmethylester 
• 97652-54-5 N-(O-Isopropyliden-D-glyceroyl)-(S-benzyl)-L-cystein 
• 97652-46-5 N-(O-Isopropyliden-D-glyceroyl)-(S-benzyl)-L-cysteinmethylester 
• 97652-49-8 N-(O-Isopropyliden-D-glyceroyl)-L-phenylalanin-tert-butylester 

Relevant academic research and scientific papers

PHENYLPYRROLIDINE COMPOUND AND USE THEREOF

Provided is a compound. The compound is a compound represented by formula (A), or a tautomer, a stereoisomer, a hydrate, a solvate, a salt, or a prodrug of the compound represented by formula (A), where R is R1 and R2 are each independently selected from H, C1-C10 alkyl, C3-C10 cycloalkyl, C1-C10 alkoxyl, halogen, and -CN; and R3, R4, and R5 are each independently selected from C1-C10 alkyl, C3-C10 cycloalkyl, C1-C10 alkoxyl, halogen, and -CN, under a premise that: if R1 is -CH3, C1, or - CN, R2 is not H, and if R1 is H, R2 is not H, -CN, or -CH3.

Oxidative Cleavage of Vicinal Diols at the Nickel Hydroxide Electrode

Vicinal diols are oxidatively cleaved with good yields by electrolysis at an oxide covered nickel electrode in an aqueous alkaline electrolyte and an undivided cell.The method is applied in the synthesis of optical pure derivatives of 2,2-dimethyl-1,3-dioxolane-4-carboxylic acid.