144425-38-7

Usage

Molecular structure

Aromatic ring system with a complex thieno[3,4-c]pyrrole core, a benzoyl group, and a 2,2-dioxide side chain.

Type of compound

Pyrrole derivative.

Molecular weight

285.32 g/mol.

Potential applications

Medicinal chemistry and pharmaceutical research.

Biological activities

Unique structure and potential biological activities, though further research is needed.

Synthesis use

Building block for the synthesis of novel organic molecules with specific properties.

Research status

Further research needed to fully understand its potential uses and biological effects.

Upstream product

• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 144425-32-1 2,2-Dioxo-2,3,4,6-tetrahydro-1H-2λ⁶-thieno[3,4-c]pyrrole-5-carboxylic acid 1-chloro-ethyl ester 
• 18214-57-8 3,4-bis-(bromomethyl)-2,5-dihydrothiophene 1,1-dioxide 
• 35105-74-9 5-benzyl-3,4,5,6-tetrahydro-1H-thieno[3,4-c]pyrrole 2,2-dioxide 
• 50586-22-6 3,4,5,6-tetrahydro-1H-thieno[3,4-c]pyrrole 2,2-dioxide 
• 144425-34-3 5-benzoyl-3,4,5,6-tetrahydro-1H-thieno<3,4-c>pyrrole 2,2-dioxide 

Downstream Products

• 144425-45-6 9-Benzoyl-1,4,5,8-tetrahydro-1,4-epiazano-naphthalene-2,3,6,7-tetracarboxylic acid tetramethyl ester 

Relevant academic research and scientific papers

New Building Blocks, 3,5-Dihydro-1H-thienopyrrole 2,2-Dioxides; Preparation and their Diels-Alder Reaction with Dimethyl Acetylenedicarboxylate

New building blocks, 3,5-dihydro-1H-thienopyrrole 2,2-dioxides 3, have been prepared by the oxidation of their corresponding pyrroline derivates 4 with DDQ or Chemical MnO2.The Diels-Alder reaction of 3 with dimethyl acetylenedicarboxylate gave new types of compounds: 7-aza-2,3-dimethylenenorbornenes A, the 1:2 adducts B, 1a,3a,6,9-tetrahydrobenzindoles C, and dihydroindolosulfolene D depending on the reaction conditions and the N-substituents.The reaction of 3 with bis(tert-butylsulfonyl)acetylene was also described.

New Building Blocks, 3,5-Dihydro-1H-thienopyrrole 2,2-Dioxides; Preparation and their Diels-Alder Reaction with Dimethyl Acetylenedicarboxylate

New building blocks, 3,5-dihydro-1H-thienopyrrole 2,2-dioxides 1, have been prepared and react with dimethyl acetylenedicarboxylate to give new types of compound; 7-aza-2,3-dimethylenenorbornene A, the 1 : 2 adduct B, 1a,3a,6,9-tetrahydrobenzindole C, and dihydroindolosulfolene D depending on the reaction conditions and the N-substituent.