CAS 2198-19-8

(2E)-1-(2-hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

Description:

The chemical substance known as (2E)-1-(2-hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one, with the CAS number 2198-19-8, is a type of chalcone, which is a class of compounds characterized by the presence of a conjugated double bond between two aromatic rings. This compound features a prop-2-en-1-one backbone, indicating it has an α,β-unsaturated carbonyl structure, which contributes to its reactivity and potential biological activity. The presence of hydroxyl (-OH) and methoxy (-OCH3) groups on the aromatic rings enhances its solubility and may influence its interaction with biological targets. Chalcones are known for their diverse pharmacological properties, including anti-inflammatory, antioxidant, and anticancer activities. The specific arrangement of substituents in this compound can affect its electronic properties and reactivity, making it a subject of interest in medicinal chemistry and organic synthesis. Additionally, its structural features may allow for various synthetic modifications, potentially leading to the development of new therapeutic agents.

Formula: C₁₇H₁₆O₄

InChI: InChI=1/C17H16O4/c1-20-13-6-3-12(4-7-13)5-10-16(18)15-9-8-14(21-2)11-17(15)19/h3-11,19H,1-2H3/b10-5+

Synonyms:

• (2E)-1-(2-Hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)-2-propen-1-one
• 2'-Hydroxy-4,4'-dimethoxychalcone
• 2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)-
• 2-propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)-, (2E)-
• (2E)-1-(2-Hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

1-(2-Hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

CAS: 2198-19-8

1-(2-Hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

Purity: ≥95%

Ref: 54-OR26085

4,4'-Dimethoxy-2'-hydroxychalcone

CAS: 2198-19-8

4,4'-Dimethoxy-2'-hydroxychalcone is a bioactive flavonoid compound, which is typically derived from plant sources such as those belonging to the family of Leguminosae. This compound operates through multifaceted mechanisms, primarily exerting its effects via modulation of cellular oxidative stress pathways and the inhibition of specific enzymes involved in inflammatory processes. By scavenging free radicals and interacting with cellular signaling pathways, it demonstrates potent antioxidant and anti-inflammatory properties.

Formula: C₁₇H₁₆O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 284.31 g/mol

Ref: 3D-FD66388