2′,4′-Dihydroxychalcone is a flavonoid compound characterized by its structure, which consists of a chalcone backbone with two hydroxyl groups located at the 2' and 4' positions of the phenyl ring. This compound is known for its potential biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. It exhibits a yellowish color and is soluble in organic solvents, making it useful in various applications, including pharmaceuticals and cosmetics. The presence of hydroxyl groups enhances its reactivity and ability to form hydrogen bonds, contributing to its biological efficacy. Additionally, 2′,4′-Dihydroxychalcone can serve as a precursor for the synthesis of other flavonoids and bioactive compounds. Its CAS number, 1776-30-3, is a unique identifier that facilitates its recognition in chemical databases and literature. Overall, this compound is of interest in both research and industrial contexts due to its diverse range of potential health benefits and applications.

2′,4′-Dihydroxychalcone

1776-30-3: 2′,4′-Dihydroxychalcone, 1-(2,4-dihydroxyphenyl)-3-phenyl-2-propen-1-on,  1-(2,4-dihydroxyphenyl)-3-phenyl-2-propen-1-one,  2’,4’-dihydroxy-chalcon,  (2E)-1-(2,4-dihydroxyphenyl)-3-phenylprop-2-en-1-one, 1-(2,4-Dihydroxyphenyl)-3-phenyl-2-propen-1-one, Chalcone, 2′,4′-dihydroxy-, 2-Propen-1-one, 1-(2,4-dihydroxyphenyl)-3-phenyl-, NSC 401492,  3-(2,4-DIHYDROXYPHENYL)-ACRYLOPHENONE

2',4'-DIHYDROXYCHALCONE (2',4'-DHC) as a compound with Hsp90 inhibitory and antifungal effects

CAS 1776-30-3: 2′,4′-Dihydroxychalcone

2',4'-DIHYDROXYCHALCONE

Ref: TM-T8829

1-(2,4-Dihydroxyphenyl)-3-Phenylprop-2-En-1-One

Ref: 54-OR1008896

2-Propen-1-one, 1-(2,4-dihydroxyphenyl)-3-phenyl-

Ref: IN-DA0025F2

2',4'-DIHYDROXYCHALCONE

Ref: 54-BUP05740