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3,5-dimethoxy-2-(4-methoxy-phenyl)-chromen-4-one is a complex organic compound belonging to the class of flavonoids, specifically a type of flavone. This molecule is characterized by a chromen-4-one core structure, which features a benzopyran ring system with a carbonyl group at the 4-position. The compound has two methoxy groups at the 3 and 5 positions of the chromen-4-one ring, and a 4-methoxy-phenyl group attached at the 2-position. This particular arrangement of functional groups endows the molecule with potential biological activities, such as antioxidant and anti-inflammatory properties, which are common among flavonoids. The compound's structure also suggests that it may have applications in the pharmaceutical and nutraceutical industries, given the diverse range of health benefits associated with flavonoids.

7736-81-4

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7736-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7736-81-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,3 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7736-81:
(6*7)+(5*7)+(4*3)+(3*6)+(2*8)+(1*1)=124
124 % 10 = 4
So 7736-81-4 is a valid CAS Registry Number.

7736-81-4Downstream Products

7736-81-4Relevant academic research and scientific papers

4'-Hydroxy-3-methoxyflavones with potent antipicornavirus activity

De Meyer,Haemers,Mishra,Pandey,Pieters,Vanden Berghe,Vlietinck

, p. 736 - 746 (2007/10/02)

4'-Hydroxy-3-methoxyflavones are natural compounds with known antiviral activities against picornaviruses such as poliomyelitis and rhinoviruses. In order to establish a structure-activity relationship a series of analogues were synthesized, and their antiviral activities and cytotoxicities were compared with those of flavones from natural origin. The 4'-hydroxyl and 3-methoxyl groups, a substitution in the 5 position and a polysubstituted A ring appeared to be essential requirements for a high activity. The most interesting compound was 4',7-dihydroxy-3-methoxy-5,6-dimethylflavone possessing in vitro TI99 values of > 1000 and > 200 against poliovirus type 1 and rhinovirus type 15, respectively. This compound was also active against other rhinovirus serotypes (2, 9, 14, 29, 39, 41, 59, 63, 70, 85, and 89) tested, having MIC50 values ranging from 0.016 to 0.5 μg/mL. Finally in contrast to quercetin it showed to be not mutagenic in concentrations up to 2.5 mg in the Ames test.

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