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Usage

Uses

Used in Pharmaceutical Industry:
3-(4-Methoxyphenyl)-1-(2-naphthyl)-prop-2-en-1-one is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of new drugs, potentially leading to advancements in medical treatments.
Used in Organic Compounds Production:
In the field of organic chemistry, 3-(4-Methoxyphenyl)-1-(2-naphthyl)-prop-2-en-1-one serves as an essential intermediate for the synthesis of a range of organic compounds. Its versatility in chemical reactions makes it valuable for creating diverse chemical products.
Used in Medicine:
Due to its biological activity, 3-(4-Methoxyphenyl)-1-(2-naphthyl)-prop-2-en-1-one holds promise for applications in medicine. While further research is required to determine its specific medical uses, its potential impact on healthcare is significant.
Used in Agriculture:
3-(4-METHOXYPHENYL)-1-(2-NAPHTHYL)-PROP-2-EN-1-ONE's biological activity also suggests potential applications within the agricultural sector. It may be utilized in the development of new pesticides, herbicides, or other agricultural chemicals to improve crop yields and protect plants from diseases and pests.

InChI:InChI=1/C20H16O2/c1-22-19-11-6-15(7-12-19)8-13-20(21)18-10-9-16-4-2-3-5-17(16)14-18/h2-14H,1H3/b13-8+

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 93-08-3 methyl 2-naphthyl ketone 
• 75-05-8 acetonitrile 
• 7228-47-9 2-(2-naphthyl)ethanol 

Downstream Products

• 113341-20-1 2-(2,6-Dichloro-phenyl)-3-(4-methoxy-phenyl)-5-naphthalen-2-yl-5-oxo-pentanenitrile 
• 127394-78-9 2-Methoxy-4-(4-methoxy-phenyl)-6-naphthalen-2-yl-nicotinonitrile 
• 127394-70-1 2-ethoxy-4-(4-methoxyphenyl)-6-(2-naphthyl)-pyridine-3-carbonitrile 
• 113341-21-2 2-(4-Chloro-phenyl)-3-(4-methoxy-phenyl)-5-naphthalen-2-yl-5-oxo-pentanenitrile 
• 113341-19-8 3-(4-Methoxy-phenyl)-5-naphthalen-2-yl-2-naphthalen-1-yl-5-oxo-pentanenitrile 
• 1438279-11-8 (S)-3-(1H-indol-3-yl)-3-(4-methoxyphenyl)-1-(naphthalen-2-yl)propan-1-one 
• 4708-38-7 naphthalen-2-yl-3-(4-methoxyphenyl)oxiran-2-yl-methanone 
• 1402658-91-6 5-(4-methoxyphenyl)-3-(naphthalen-2-yl)-4,5-dihydropyrazole-1-carbothioamide 
• 1402658-59-6 3-{2-[5-(4-methoxyphenyl)-3-naphthalen-2-yl-4,5-dihydropyrazol-1-yl]-4-oxo-4,5-dihydro-1,3-thiazol-5-ylidene}-2,3-dihydro-1H-indol-2-one 
• 114346-60-0 C₂₀H₁₈N₂O 
• 1402658-85-8 5-Chloro-3-[5-(4-methoxyphenyl)-3-naphthalen-2-yl-pyrazol-1-yl]-2,3-dihydro-1H-indol-2-one 
• 1402658-84-7 3-[5-(4-methoxyphenyl)-3-naphthalen-2-ylpyrazol-1-yl]-2,3-dihydro-1H-indol-2-one 
• 1402658-60-9 5-bromo-3-{2-[5-(4-methoxyphenyl)-3-naphthalen-2-yl-4,5-dihydropyrazol-1-yl]-4-oxo-4,5-dihydro-1,3-thiazol-5-ylidene}-2,3-dihydro-1H-indol-2-one 

Relevant academic research and scientific papers

Synthesis, Biological Activity and Action Mechanism Study of Novel Chalcone Derivatives Containing Malonate

A series of novel chalcone malonate derivatives were synthesized and their antibacterial and antiviral activities were evaluated. All target compounds were characterized by spectral data. The results of antimicrobial bioassay showed that one compound (die

Investigating the Anticancer Activity of Isatin/Dihydropyrazole Hybrids

A series of isatin-dihydropyrazole hybrids have been synthesized in order to assess their potential as anticancer agents. In particular, 12 compounds were evaluated for their antiproliferative activity toward A549, IGR39, U87, MDA-MB-231, MCF-7, BT474, Bx

Effect of ring A and ring B substitution on the cytotoxic potential of pyrazole tethered chalcones

Chalcone is an aromatic ketone that forms the central core for a variety of important biological compounds, which are collectively known as chalcones. The cytotoxic potential of chalcones which consists of C6-C 3-C6 units gets enhanced by the incorporation of pyrazole ring as proved by our earlier studies. Thus in the present work, pyrazoles of chalcones with ring A substituted by furan, naphthalene and variety of substituted phenyl rings has been prepared and evaluated for in vitro cytotoxic activity against PC-3, OVCAR, IMR-32, HEP-2 human cancer cell lines. Springer Science+Business Media, LLC 2011.

Tetrachlorosilane-zinc chloride as a new potent binary reagent for one-pot, three-component synthesis of mannich-type products

A combination of tetrachlorosilane and zinc chloride in dichloromethane as an efficient and ambient binary reagent to promote a one-pot amidoalkylation reaction of enolizable ketones, aromatic aldehydes with acetonitriles, or benzonitrile have been develo

Microwave-assisted synthesis of some 3,5-arylated 2-pyrazolines

Condensation of 2-acetylnaphthalene with benzaldehydes under microwave irradiation affords chalcones which undergo facile and clean cyclizations with hydrazines RNHNH2 (R= H, Ph, Ac) to afford 3,5-arylated 2-pyrazolines in quantitative yields,