3-(2-Furanyl)-1-phenyl-2-propen-1-one, also known as furyl chalcone, is an organic compound characterized by its unique structure that includes a furan ring and a phenyl group attached to a propenone moiety. This compound typically exhibits a yellow to orange color and is known for its potential applications in various fields, including organic synthesis and medicinal chemistry. Furyl chalcone is recognized for its ability to undergo various chemical reactions, such as condensation and polymerization, due to the presence of the α,β-unsaturated carbonyl group. It may also exhibit biological activities, including antioxidant and anti-inflammatory properties, making it of interest in pharmaceutical research. The compound is generally soluble in organic solvents, and its reactivity can be influenced by the presence of substituents on the aromatic rings. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.

3-(2-Furanyl)-1-phenyl-2-propen-1-one

717-21-5: 1,1'-(2E)-but-2-ene-2,3-diyldibenzene, 1-(3-Furan-2-Ylphenyl)Prop-2-En-1-One, 2-Furfurylideneacetophenone, 2-Propen-1-one, 3-(2-furanyl)-1-phenyl-, 2-Propen-1-one, 3-(2-furanyl)-1-phenyl- (9CI), 3-(2-Furanyl)-1-phenyl-2-propen-1-one, 3-(2-Furyl)-1-phenyl-2-propen-1-one, Acrylophenone, 3-(2-furyl)-, Ai3-04601, Brn 0134154, Furfuralacetophenone, Furfurylideneacetophenone, Nsc 2049,  5-17-10-00371 (Beilstein Handbook Reference),  3-(2-Furyl)acrylophenone, 3-(2-Furyl)acrylophenone

2-Furylprop-2-en-1-one is a valency compound that has an electron configuration of 2. It is a chalcone with an alcohol group, which makes it a cycloaliphatic compound. Its presence in cells has been shown to be due to its ability to bind with the chloride ion and form an anion. This anion can then react with other molecules to form a dipole or hydrogen bond, which allows it to interact with other compounds. 2-Furylprop-2-en-1-one also reacts with hydroxy groups and hydroxyl groups, which are found in proteins that are important for cellular functions such as protein synthesis. The molecule also interacts with acceptors such as naphthalene and acetyl derivatives.

CAS 717-21-5: 3-(2-Furanyl)-1-phenyl-2-propen-1-one

3-(2-Furanyl)-1-phenyl-2-propen-1-one

Ref: 3B-F1373

(2E)-3-(2-Furyl)-1-phenylprop-2-en-1-one

Ref: 3D-FF120369

(2E)-3-(2-furyl)-1-phenylprop-2-en-1-one

Ref: 10-F368154