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3-hydroxy-2,3,7-trimethoxy-2-phenyl-2,3-dihydro-4H-chromen-4-one is a complex organic compound with a molecular formula of C18H18O6. It is a derivative of flavonoids, a class of natural products that are widely found in plants and exhibit various biological activities, such as antioxidant, anti-inflammatory, and anticancer properties. This specific compound features a chromenone core structure, with a hydroxyl group at the 3-position, three methoxy groups at the 2, 3, and 7 positions, and a phenyl group at the 2-position. The compound is known for its potential therapeutic applications, particularly in the treatment of various diseases, due to its ability to modulate cellular processes and interact with biological targets. Its chemical structure and properties make it a subject of interest in the field of medicinal chemistry and natural product research.

2047-54-3

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2047-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2047-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2047-54:
(6*2)+(5*0)+(4*4)+(3*7)+(2*5)+(1*4)=63
63 % 10 = 3
So 2047-54-3 is a valid CAS Registry Number.

2047-54-3Relevant academic research and scientific papers

Oxidation of Flavonols using lead(IV) acetate in acidic methanol

Kumar,Singh

, p. 1333 - 1337 (2007/10/02)

Oxidation of Flavonols (1a-h) and 6-propionylflavonols (1i-j) to 2,3-dimethoxy-3-hydroxyflavanones (2a-h) and 2,3-dimethoxy-3-hydroxyflavanones (2i-j), respectively using lead(IV) acetate in methanol in presence of perchloric acid and the mechanism of this transformation has been described.

HYPERVALENT IODINE OXIDATION OF FLAVONOLS USING BENZENE IN METHANOL

Moriarty, Robert M.,Prakash, Om,Musallam, Hikmat A.,Mahesh, Vijendra K.

, p. 1641 - 1645 (2007/10/02)

Hypervalent iodine oxidation of various flavonols (1a-1f) and α-naphthoflavonol (3) using benzene (HTIB) in methanol leads to the formation of 2,3-dimethoxy-3-hydroxyflavanones (2a-2f) and 2,3-dimethoxy-3-hydroxy-α-naphthoflavanone (4) respectively.HTIB resembles periodic acid in its oxidative behavior towards flavonols.

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