79325-08-9

Basic information

• Product Name: 1-(4-CHLOROPHENYL)-3-(3,4-DICHLOROPHENYL)PROP-2-EN-1-ONE
• Synonyms: 1-(4-CHLOROPHENYL)-3-(3,4-DICHLOROPHENYL)PROP-2-EN-1-ONE
• CAS NO: 79325-08-9
• Molecular Formula: C₁₅H₉Cl₃O
• Molecular Weight: 311.59
• Mol File: 79325-08-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-CHLOROPHENYL)-3-(3,4-DICHLOROPHENYL)PROP-2-EN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-CHLOROPHENYL)-3-(3,4-DICHLOROPHENYL)PROP-2-EN-1-ONE(79325-08-9)
• EPA Substance Registry System: 1-(4-CHLOROPHENYL)-3-(3,4-DICHLOROPHENYL)PROP-2-EN-1-ONE(79325-08-9)

Safety Data

• Hazardous Substances Data: 79325-08-9(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 15 carbon (C) atoms, 9 hydrogen (H) atoms, 3 chlorine (Cl) atoms, and 1 oxygen (O) atom.

Explanation

The compound is a solid at room temperature and has a yellow color. Its crystalline structure gives it a powdery texture.

Explanation

Chalcones are a type of chemical structure that consist of two aromatic rings connected by a three-carbon chain containing a carbon-carbon double bond. This specific compound has a 4-chlorophenyl group and a 3,4-dichlorophenyl group attached to the three-carbon chain.

Explanation

Chalcones are known for their diverse biological activities, which include anti-inflammatory, antioxidant, and anticancer properties. The specific biological activities of this compound may be influenced by its unique chemical structure.

Explanation

Due to its unique chemical structure and potential biological activities, this compound can be used as a starting material or intermediate in the synthesis of other organic compounds. It may also be studied for its potential therapeutic applications in the pharmaceutical industry.

Explanation

The reactivity of this compound is influenced by its chemical structure, particularly the presence of the chlorine atoms and the carbon-carbon double bond. These functional groups can participate in various chemical reactions, such as electrophilic aromatic substitution, nucleophilic addition, and oxidation.

Explanation

While the compound has potential applications in organic synthesis and pharmaceutical research, more research is required to fully understand its properties, reactivity, and potential uses in various fields. This may involve studying its interactions with other molecules, its stability under different conditions, and its potential effects on biological systems.

Appearance

Yellow crystalline powder

Chemical structure

Chalcone

Biological activities

Various

Applications

Organic synthesis and pharmaceutical research

Reactivity

Determined by chemical structure

Further research

Needed to understand potential uses

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 2642-63-9 3',4'-dichloroacetophenone 

Downstream Products

• 170939-62-5 [4-(4-Chloro-phenyl)-1H-pyrrol-3-yl]-(3,4-dichloro-phenyl)-methanol 
• 170939-27-2 [4-(4-Chloro-phenyl)-1H-pyrrol-3-yl]-(3,4-dichloro-phenyl)-methanone 
• 78807-78-0 2-[3-(4-Chloro-phenyl)-5-(3,4-dichloro-phenyl)-4,5-dihydro-pyrazol-1-yl]-1-phenothiazin-10-yl-ethanone 

Relevant articles and documents

Synthesis and insect antifeedant activities of some substituted styryl 3,4-dichlorophenyl ketones

Sixteen substituted styryl 3,4-dichlorophenyl ketones [(2E)-1-(3,4-dichlorophenyl)-3-phenyl-2-propen-1-ones] were synthesized using eco-friendly benign stereoselective crossed-aldol reaction. They are characterized by their analytical, infrared, NMR and m

Synthesis and Biological Activity of Some New 10-phenothiazines

Fourteen 10-phenothiazines (IV) have been synthesized via condensation of 10-hydrazino-acetylphenothiazine with substituted benzalacetophenones.These compounds inhibit 33-86percent in vitro activity of rat brain pyruvate oxidase and afford protection against pentylenetetrazol induced seizures in albino mice.However, their anticonvulsant properties are found to be independent of their pyruvate oxidase inhibitory activity.