6271-22-3

Usage

Uses

Used in Pharmaceutical Industry:
(4E)-1,5-diphenylpent-4-ene-1,3-dione is used as a starting material for the preparation of various pharmaceuticals due to its potential biological activities, including antioxidant and anti-inflammatory properties. It is a subject of interest for researchers in the fields of medicinal chemistry and pharmacology for its potential use in the treatment of various diseases.
Used in Agrochemical Industry:
(4E)-1,5-diphenylpent-4-ene-1,3-dione is also used as a starting material for the preparation of various agrochemicals, contributing to the development of new and effective products in this industry.
Used in Organic Synthesis:
(4E)-1,5-diphenylpent-4-ene-1,3-dione serves as a reactant in organic synthesis, allowing for the creation of a wide range of chemical compounds and products. Its versatility in this field makes it valuable for researchers and chemists working on various projects.

Upstream product

• 102-92-1 cinnamoyl chloride 
• 98-86-2 acetophenone 
• 4192-77-2 ethyl cinnamate 
• 538-58-9 1,5-diphenyl-1,4-pentadiene-3-one 
• 104-55-2 3-phenyl-propenal 
• 70-11-1 α-bromoacetophenone 
• 621-82-9 Cinnamic acid 
• 854029-40-6 4,5-dibromo-1,5-diphenyl-pent-1-en-3-one 
• 58225-28-8 2-bromo-1,5-diphenyl-penta-1,4-dien-3-one 
• 7732-18-5 water 
• 27271-22-3 3-Aethoxy-1,5-diphenyl-2,4-pentadien-1-on 
• 27271-21-2 C₃₀H₂₇O₂P 
• 100-52-7 benzaldehyde 

Downstream Products

• 621-82-9 Cinnamic acid 
• 98-86-2 acetophenone 
• 1441-42-5 3-phenyl-5-styrylisoxazole 
• 858859-05-9 4,5-dibromo-1,5-diphenyl-pentane-1,3-dione 
• 1029-94-3 2,6-diphenyl-pyran-4-one 
• 1226972-77-5 C₂₇H₂₀N₂O₂ 

Relevant academic research and scientific papers

Europium complex, ligand thereof and polypropylene luminescent material doped with europium complex

The invention discloses a europium complex and a europium complex doped polypropylene luminescent material. The structures of the europium complex and a ligand of the europium complex are shown in formulas II and I. The preparation method of the long conj

Nucleophilic acylation of α-haloketones with aldehydes: An umpolung strategy for the synthesis of 1,3-diketones

The first example of N-heterocyclic carbene (NHC)-promoted intermolecular acylation of α-haloketones with aldehydes and α,β-unsaturated aldehydes (enals) is reported. The protocol involves carbonyl umpolung reactivity of aldehydes and enals in which the carbonyl carbon attacks nucleophilically on electrophilic terminal of α-haloketones to afford 1,3-diketones and α,β-unsaturated 1,3-diketones, respectively. Short reaction time, ambient temperature, operational simplicity, and high yields are the salient features of the present procedure.

NEW METHOD FOR PRODUCING α,β-UNSATURATED β-DIKETONES

This paper proposes a new method for obtaining α,β-unsaturated acyclic β-diketones that differs from existing techniques in utilizing simple technology and giving high target product yields.

Pharmaceutical compositions containing 5-phenyl-1,3-dioxoalkenyl compounds

This invention relates to pharmaceutical compositions containing a class of 5-phenyl-1,3-dioxoalkenyl compounds useful as inhibitors of leukotriene biosynthesis and thus useful in the treatment of conditions associated with leukotrienes. This invention al