5336-78-7

Usage

Uses

Used in Organic Synthesis:
(2E)-3-phenyl-1-(4-[(1E)-phenylmethylidene]aminophenyl)prop-2-en-1-one is used as a reagent in chemical reactions for the synthesis of complex organic molecules. Its unique structure allows it to participate in various chemical reactions, making it a valuable component in the creation of new compounds.
Used in Pharmaceutical Research:
(2E)-3-phenyl-1-(4-[(1E)-phenylmethylidene]aminophenyl)prop-2-en-1-one has potential medical or pharmaceutical uses, although further research is needed to fully understand its properties and potential applications. Its unique chemical structure may offer new avenues for the development of pharmaceuticals and other medical treatments.
Used in Chemical Research:
(2E)-3-phenyl-1-(4-[(1E)-phenylmethylidene]aminophenyl)prop-2-en-1-one is also used in chemical research to study the properties and reactions of ketone compounds containing phenyl rings and amino groups. This research can lead to a better understanding of the behavior of these types of compounds and their potential applications in various fields.

Upstream product

• 100-52-7 benzaldehyde 
• 99-92-3 p-aminobenzophenone 
• 64-17-5 ethanol 

Downstream Products

• 2403-30-7 4'-aminochalcone 
• 10179-72-3 5-(4-acetamidophenyl)-1,3-diphenyl-2-pyrazoline 
• 42558-04-3 4-(5-Phenyl-4,5-dihydro-1H-pyrazol-3-yl)-phenylamine 
• 77153-29-8 (cis)-1-(p-Aminophenyl)-2-phenylcyclopropane 
• 42557-87-9 (trans)-1-(p-Aminophenyl)-2-phenylcyclopropane 

Relevant academic research and scientific papers

Synthesis of Some New &β-Lactams, 4-Thiazolidinones and Pyrazolines

N-Arylidene-p-aminoacetophenone (I) and N-arylidene-4'-aminochalcones (V) have been converted into a series of substituted β-lactams (III) and 4-thiazolidinones (IV), and pyrazolines (VI, VII) respectively. p-Chloroacetamidoacetophenone (II) has also been converted into series of substituted 4'-piperidino/morpholinoacetoamidochalcones (X) which undergo cyclization on treatment with hydrazine, phenylhydrazine or thiourea to pyrazolines (XI, XII) and pyrimidine-2-thiones (XIII) respectively.The antibacterial and antifungal activities of the compounds have been determined.

Kinetic Study of the Homolytic Brominolysis of 1,2-Diarylcyclopropanes

The rate constants for the photolytic brominolysis of 22 trans-1,2-diarylcyclopropanes in carbon disulfide relative to an internal standard, p-chlorotoluene, have been determined.The products of the brominolysis are 1,3-dibromo-1,3-diarylpropanes.The rate constants range over 5 orders of magnitude, being enhanced by electrondonating substituents on one or both benzene rings.The quantitative size of the substituent effect (ρ) at either involved carbon center is a function of the substituent at the other center.This fact suggests a continuum of transition-state structures with varying degrees of bond breaking and charge separation.