116854-95-6

Basic information

• Product Name: Ethanone, 2-(2-methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)-
• CAS NO: 116854-95-6
• Molecular Formula: C15H14O5
• Molecular Weight: 274.273
• Mol File: 116854-95-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(2-methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(2-methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)-(116854-95-6)
• EPA Substance Registry System: Ethanone, 2-(2-methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)-(116854-95-6)

Safety Data

• Hazardous Substances Data: 116854-95-6(Hazardous Substances Data)

Usage

General Description

Ethanone, 2-(2-methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)-, also known as hesperetin, is a flavonoid compound found in citrus fruits such as oranges and lemons. It has been studied for its potential therapeutic properties, including antioxidant, anti-inflammatory, anti-cancer, and neuroprotective effects. Hesperetin has been found to have a high antioxidant capacity, which may help protect cells from damage caused by free radicals. It also has potential anti-inflammatory properties, which could make it useful for conditions involving inflammation such as arthritis. Additionally, hesperetin has shown promise for its anti-cancer effects, potentially inhibiting the growth of cancer cells. Overall, research on hesperetin suggests it may have a variety of health benefits and could be a valuable compound for further study in the field of natural medicine and pharmaceuticals.

Upstream product

• 108-73-6 3,5-dihydroxyphenol 
• 7035-03-2 2-methoxy-benzeneacetonitrile 

Downstream Products

• 247564-48-3 5,7-dihydroxy-3-(2-methoxy-phenyl)-4-oxo-4H-chromene-2-carboxylic acid ethyl ester 
• 342643-54-3 1-(2-hydroxy-4,6-bis-methoxymethoxy-phenyl)-2-(2-methoxy-phenyl)-ethanone 
• 247564-47-2 5,7-dihydroxy-3-(2-methoxyphenyl)-4H-chromen-4-one 
• 70943-68-9 Irilin C 
• 1445712-03-7 7-hydroxy-5-methoxy-3-(2-methoxyphenyl)-8-(morpholin-4-ylmethyl)-4H-chromen-4-one 
• 1445711-93-2 7-hydroxy-8-[(4-methylpiperazin-1-yl)methyl]-5-methoxy-3-(2-methoxyphenyl)-4H-chromen-4-one 
• 1445711-87-4 7-hydroxy-5-methoxy-3-(2-methoxyphenyl)-8-(piperidin-1-ylmethyl)-4H-chromen-4-one 
• 1445711-60-3 7-hydroxy-5-methoxy-3-(2-methoxyphenyl)-4H-chromen-4-one 
• 1445711-50-1 5-methoxy-3-(2-methoxyphenyl)-4-oxo-4H-chromen-7-yl dimethylcarbamate 
• 1445711-40-9 5-hydroxy-3-(2-methoxyphenyl)-4-oxo-4H-chromen-7-yl dimethylcarbamate 
• 5065-01-0 5,7-dimethoxy-3-(2-methoxy-phenyl)-chromen-4-one 
• 56308-08-8 2-Hydroxy-3,4-dimethoxyphenyl 2-methoxybenzyl ketone 
• 789493-47-6 2-hydroxy-4,6,2'-trimethoxy-3-methyl-deoxybenzoin 

Relevant articles and documents

Synthesis and aminomethylation of 7-hydroxy-5-methoxyisoflavones

A synthetic method for 7-hydroxy-5-methoxyisoflavones starting from 5,7-dihydroxyisoflavones was developed. Dimethylcarbamoylchloride was proposed for protection of the 7-hydroxy group. Aminomethylation of the synthesized 7-hydroxy-5-methoxyisoflavones by formaldehyde aminals was studied.

Synthesis of analogs of natural isoflavonoids containing phloroglucinol

Analogs of the natural isoflavonoids biochanin A and orobol were synthesized. Alkylation involving phenolic hydroxyls and the chromone ring was studied.