3437-29-4

Usage

Uses

Used in Pharmaceutical Research and Organic Synthesis:
3,3-Dimethylpyrrolidine-2,5-dione is used as an intermediate in the synthesis of various pharmaceutical compounds, including antipsychotic medications and central nervous system drugs. Its unique structure and properties make it a valuable building block for developing new and effective medications.
Used in Agricultural Chemicals Production:
3,3-Dimethylpyrrolidine-2,5-dione is utilized as a key component in the production of agricultural chemicals. Its incorporation into these products helps enhance their effectiveness in protecting crops and improving agricultural yields.
Used in Dye Production:
3,3-Dimethylpyrrolidine-2,5-dione is employed as a building block in the synthesis of dyes, contributing to the development of new and innovative colorants for various industries, including textiles, plastics, and printing.

Upstream product

• 463-82-1 2,2-dimethylpropane 
• 82621-77-0 2,2-dimethyl-N-bromosuccinimide 

Downstream Products

• 3437-30-7 3,3-dimethylpyrrolidine 
• 4479-75-8 3-methyl-2-butenamide 
• 86106-26-5 1-Cyclohex-3-enylmethyl-3,3-dimethyl-pyrrolidine-2,5-dione 
• 113661-36-2 N-(p-methoxytrityl)-2,2-dimethylsuccinimide 
• 597-43-3 2,2-dimethylsuccinic acid 
• 4831-43-0 3,3-dimethylpyrrolidin-2-one 
• 86106-63-0 N-(cyclohex-3-enylmethyl)-5-hydroxy-4,4-dimethylpyrrolidin-2-one 
• 113661-37-3 (RS)-N-(p-methoxytrityl)-2,2,3-trimethylsuccinimide 
• 113661-38-4 (RS)-2-allyl-N-(p-methoxytrityl)-3,3-dimethylsuccinimide 
• 792915-20-9 3,3-dimethylpyrrolidine hydrochloride 
• 1431332-59-0 C₁₂H₁₆ClN 
• 1431332-61-4 C₁₂H₁₆ClN 
• 1431332-63-6 C₁₂H₁₆ClN 
• 1431332-65-8 C₁₂H₁₅Cl₂N 

Relevant academic research and scientific papers

Ground- and Excited-State Succinimidyl Radicals in Chain Reactions: A Reexamination

The succinimidyl radical chemistry reported earlier and previously attributed to the ? state is reproduced, leaving unsettled only its assignment to the ? and ? state.This chemistry, observed in the presence of small amounts of alkenes which scavenge bromine, includes the following: (1) additions to alkenes, (2) additions to arenes, (3) Cl-like substitution selectivities, and (4) ring-openings.The chemistry previously reported under the title "?" is neither as simple nor conclusive as thought earlier.As reported earlier, ring-opening is suppressed by inclusion of bromine, benzene, bromotrichloromethane, or larger amounts of alkenes.These observations indicate the presence of a different chain carrier, formerly labeled as S?.We show now that the S? explanation was not correct with addends benzene, bromotrichloromethane, and olefins, and we identify the specific competitive processes.Reactions in the presence of bromine still show evidence for a third hydrogen abstractor besides an imidyl radical and a bromine atom.At this time there is no unambiguous identification of this third chain intermediate.