6802-49-9

Usage

Uses

Used in Pharmaceutical Industry:
7,3'-DIMETHOXYFLAVONE is used as a pharmaceutical agent for its diverse pharmacological properties. Its ability to bind to biomolecules, chelate metal ions, and scavenge free radicals makes it a promising candidate for the development of drugs targeting various diseases and conditions.
Used in Nutraceutical Industry:
7,3'-DIMETHOXYFLAVONE is used as a nutraceutical ingredient due to its antioxidant and free radical scavenging properties. It can be incorporated into dietary supplements and functional foods to promote health and well-being.
Used in Cosmetic Industry:
7,3'-DIMETHOXYFLAVONE is used as an active ingredient in cosmetic products for its potential skin health benefits. Its antioxidant and free radical scavenging properties may help protect the skin from environmental damage and promote a youthful appearance.
Used in Agricultural Industry:
7,3'-DIMETHOXYFLAVONE can be used in the agricultural industry as a natural pesticide or growth promoter. Its ability to bind to biomolecules and chelate metal ions may provide protection against pests and enhance crop growth.
Used in Food and Beverage Industry:
7,3'-DIMETHOXYFLAVONE can be used as a natural food additive for its antioxidant properties. It can help preserve the freshness and quality of food products while also providing potential health benefits to consumers.

InChI:InChI=1/C17H14O4/c1-19-12-5-3-4-11(8-12)16-10-15(18)14-7-6-13(20-2)9-17(14)21-16/h3-10H,1-2H3

Upstream product

• 32272-16-5 7-methoxy-2-(3-methoxyphenyl)chroman-4-one 
• 32329-98-9 3,4'-Dimethoxy-2'-Hydroxychalcone 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 1371663-77-2 C₁₇H₁₆O₅ 
• 586-38-9 3-Methoxybenzoic acid 

Downstream Products

• 1371663-59-0 4-(2-hydroxy-4-methoxyphenyl)-6-(3-methoxyphenyl)-2-aminopyrimidine 
• 108238-40-0 7,3'-dihydroxyflavone 
• 145370-50-9 7-hydroxy-3'-methoxyflavone 
• 320576-70-3 2-(3-hydroxy-phenyl)-7-methoxy-chromen-4-one 

Relevant academic research and scientific papers

Synthesis method of 2-aminopyrimidine antiplatelet compound

The invention discloses a synthesis method of a 2-aminopyrimidine antiplatelet compound, and the synthesis method comprises the following steps: selecting o-hydroxybenzaldehyde A and 2-bromoacetophenone B containing different substituent groups as raw materials, taking nitrogen heterocyclic carbene as a reaction catalyst, synthesizing an intermediate 1,3-diketone compound C of a novel antiplateletdrug under an alkaline condition, then synthesizing a flavonoid compound D under an acidic condition by the 1,3-diketone compound C, and finally generating the end product 2-aminopyrimidine antiplatelet compound E by the flavonoid compound D and guanidine hydrochloride under an alkaline condition. The synthesis method simplifies the original synthesis method from four steps to three steps, greatly simplifies the original synthesis method, thereby effectively reducing the production cost and the price of medicines, and improving the possibility for industrial production.

Assessment of antiplatelet activity of 2-aminopyrimidines

A series of 4,6-diaryl-2-aminopyrimidines was developed as antiplatelet agents and their potency was evaluated by in vitro assay. Compound 14k was found to be two times more potent than aspirin. These encouraging results could be helpful for the development of new antiplatelet compounds.

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation

A general route for the synthesis of biologically important flavones is reported via a two step sequence employing a catalytic Wacker-Cook oxidation4b as the key step.

A Facile Preparation of Flavones Using Nonaqueous Cation-Exchange Resin

Flavone was prepared from 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione by using nonaqueous cation exchange resin in a nearly quantitative yield.Of several reaction media, isopropyl alcohol gave the best result.Eight substituted flavones were also synthesized from the corresponding diketones in satisfactory yields.

Cyclodehydrogenation of 2'-Hydroxychalcones with DDQ: A Simple Route for Flavones and Aurones

The oxidation of 2'-hydroxychalcones with 2,3-dichloro-5,6-dicyano-p-benzoquinone provides a useful synthetic route for flavones and aurones.

Utilization of "2-Pyrrolidone Hydrotribromide" in the Synthesis of Flavones

The reaction of flavanone with "2-pyrrolidone hydrotribromide" in tetrahydrofuran gave 3-bromoflavanone in a good yield.On the other hand, flavone was obtained in 97percent yield when this reaction was carried out in dimethyl sulfoxide at 80 deg C.Under the same conditions, most flavones were obtained from the corresponding flavanones in high purity and good yiels.