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3-(4-Dimethylamino-anilino)-flavon, also known as 3-(4-dimethylaminophenyl)-2-phenyl-1-benzofuran-4,7-diol, is a synthetic organic compound belonging to the flavonoid class. It is characterized by a flavone skeleton with a 4-dimethylaminophenyl group attached to the 3-position and a hydroxyl group at the 7-position. 3-(4-Dimethylamino-anilino)-flavon exhibits a range of biological activities, including antioxidant, anti-inflammatory, and anticancer properties. Its chemical structure endows it with the ability to interact with various biological targets, making it a subject of interest in pharmaceutical research. The compound's potential applications span from the development of new drugs to the study of its mechanisms of action in cellular processes.

5526-51-2

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5526-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5526-51-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5526-51:
(6*5)+(5*5)+(4*2)+(3*6)+(2*5)+(1*1)=92
92 % 10 = 2
So 5526-51-2 is a valid CAS Registry Number.

5526-51-2Downstream Products

5526-51-2Relevant academic research and scientific papers

Synthesis of trans-2,3-dimethoxy-3-(phenylamino)flavanones and related compounds

De, Surya K.,Dhara, Mrinal G.,Mallik, Asok K.

, p. 199 - 204 (2007/10/03)

trans-2,3-Dimethoxy-3-(phenylamino)flavanones (2), a new type of flavanone derivatives, are synthesized from flavanones or 2′-hydroxychalcones in two steps, the first one being a condensation with nitrosobenzenes (Ehrlich-Sachs reaction) and the second an oxidation with (diacetoxyiodo)benzene in methanol. Nitrone formation, an important side reaction of the Ehrlich-Sachs reaction, has also been exploited to synthesize 2 simply by use of an excess of nitrosobenzene in aqueous methanol. Syntheses of several analogues of 2 are also reported.

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