CAS 6272-43-1
:3-(3,4-Dihydroxyphenyl)-1-(2-hydroxyphenyl)-2-propen-1-one
Description:
3-(3,4-Dihydroxyphenyl)-1-(2-hydroxyphenyl)-2-propen-1-one, commonly known as a type of chalcone, is an organic compound characterized by its structure, which features a conjugated system of double bonds and aromatic rings. This compound typically exhibits a yellow to orange color, indicative of its chromophoric properties. It is known for its potential biological activities, including antioxidant, anti-inflammatory, and antimicrobial effects, making it of interest in pharmaceutical and nutraceutical research. The presence of multiple hydroxyl groups enhances its reactivity and solubility in polar solvents, while also contributing to its ability to form hydrogen bonds. Additionally, chalcones like this one can undergo various chemical transformations, such as cyclization and oxidation, which can lead to the formation of more complex structures. Its applications may extend to fields such as organic synthesis, materials science, and medicinal chemistry, where it can serve as a precursor or building block for more complex molecules.
Formula:C15H12O4
InChI:InChI=1S/C15H12O4/c16-12-4-2-1-3-11(12)13(17)7-5-10-6-8-14(18)15(19)9-10/h1-9,16,18-19H
InChI key:InChIKey=PSYVAIWGYVDYHN-UHFFFAOYSA-N
SMILES:C(C=CC1=CC(O)=C(O)C=C1)(=O)C2=C(O)C=CC=C2
Synonyms:- 2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(2-hydroxyphenyl)-
- 2-propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(2-hydroxyphenyl)-, (2E)-
- 2′,3,4-Trihydroxychalcone
- 3,4,2′-Trihydroxychalcone
- 3-(3,4-Dihydroxyphenyl)-1-(2-hydroxyphenyl)-2-propen-1-one
- Chalcone, 2′,3,4-trihydroxy-
- NSC 37433
- (2E)-3-(3,4-Dihydroxyphenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one
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Found 2 products.
3-(3,4-Dihydroxyphenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one
CAS:3-(3,4-Dihydroxyphenyl)-1-(2-hydroxyphenyl)prop-2-en-1-onePurity:≥95%Molecular weight:256.25g/mol2',3,4-Trihydroxychalcone
CAS:<p>2',3,4-Trihydroxychalcone is a chalcone compound, which is a type of flavonoid. Chalcones are aromatic ketones and are characterized by the presence of two phenyl rings connected by a three-carbon α,β-unsaturated carbonyl system. This compound, specifically, is known for its multiple hydroxyl groups at the 2', 3, and 4 positions on the A-ring, contributing to its chemical reactivity.</p>Formula:C15H12O4Purity:Min. 95%Color and Shape:Orange PowderMolecular weight:256.25 g/mol

