118922-13-7

Usage

Uses

Used in Organic Synthesis:
(E,E)-N-Phenylsulfonyl-4-phenyl-1-aza-1,3-butadiene is used as a versatile building block in organic synthesis for the construction of complex molecular structures. Its application is due to its ability to participate in various reactions, such as Diels-Alder and Michael additions, to create diverse functionalized products.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (E,E)-N-Phenylsulfonyl-4-phenyl-1-aza-1,3-butadiene is used as a key intermediate for the development of new drugs. Its application is attributed to its unique structure and reactivity, which facilitate the creation of novel molecular entities with potential therapeutic properties.
Used in Agrochemicals:
(E,E)-N-Phenylsulfonyl-4-phenyl-1-aza-1,3-butadiene is also utilized as a building block in the agrochemical industry for the synthesis of new compounds with pesticidal or herbicidal activities. Its application is due to its potential to be incorporated into various chemical structures with desired biological properties.
Used in Materials Science:
In the field of materials science, (E,E)-N-Phenylsulfonyl-4-phenyl-1-aza-1,3-butadiene is used as a component in the development of new materials with specific properties. Its application is based on its ability to contribute to the formation of complex molecular structures with potential applications in various industries.
Used in Medicinal Chemistry:
(E,E)-N-Phenylsulfonyl-4-phenyl-1-aza-1,3-butadiene is used as a promising candidate in medicinal chemistry for its potent biological activities, such as antimicrobial and antifungal properties. Its application is due to the potential for further investigation and development into new therapeutic agents.

Upstream product

• 98-10-2 benzenesulfonamide 
• 104-55-2 3-phenyl-propenal 
• 14371-10-9 (E)-3-phenylpropenal 

Downstream Products

• 118922-03-5 (2R,3R,4R)-1-Benzenesulfonyl-2-benzyloxy-3-methyl-4-phenyl-1,2,3,4-tetrahydro-pyridine 
• 118922-03-5 (2R,3R,4S)-1-Benzenesulfonyl-2-benzyloxy-3-methyl-4-phenyl-1,2,3,4-tetrahydro-pyridine 
• 118922-03-5 (2R^*,3S^*,4R^*)-2-(benzyloxy)-3-methyl-4-phenyl-1-(phenylsulfonyl)-1,2,3,4-tetrahydropyridine 

Relevant academic research and scientific papers

Transition metal complexes in organic synthesis. Part 57: Synthesis of 1-azabuta-1,3-dienes and application to catalytic complexation of buta-1,3- dienes and cycloalkadienes by the tricarbonyliron fragment

The 1-azabuta-1,3-dienes 5a-g were prepared and transformed to the corresponding tricarbonyliron complexes 6. The efficiency of 6 as tricarbonyliron transfer reagents and the activity of 5a-g for the catalytic complexation with either nonacarbonyldiiron o

Cycloaddition Reactions of N-Phenylsulfonyl-1-azabuta-1,3-dienes with Mesoionic 2,4-Diphenyl-1-methyl-1,3-oxazolium 5-oxide

N-Phenylsulfonyl unsaturated imines (1) react with 2,4-diphenyl-3-methyl-1,3-oxazolium 5-oxide (2) giving 4-styrylimidazoles (3), open chain products (4) and pyrrol-3-ylcarboxaldehyde N-phenylsulfonylimines (5).The mechanism of formation of all the produc

Inverse electron demand Diels-Alder reactions of N-sulfonyl α,β-unsaturated imines: A general approach to implementation of the 4π participation of 1-aza-1,3-butadienes in Diels-Alder reactions

Full details of a study of the inverse electron demand Diels-Alder reactions of W-sulfonyl-1 -aza-1,3-tmtadienes are described. The α,β-unsaturated N-sulfonylimines proved accessible through clean, homolytic rearrangement of in situ generated oxime O-sulf