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α-Hydroxy-2',4'-dimethoxy-4-methoxymethoxydihydrochalcone is a complex organic compound with the molecular formula C18H22O7. It is a type of chalcone, which is a class of flavonoids known for their diverse biological activities. This specific chalcone is characterized by the presence of a hydroxyl group (-OH) at the α-position, and three methoxy groups (-OCH3) at the 2', 4', and 4-positions. The 4-methoxymethoxy group indicates an additional methoxy group attached to a methoxymethoxy moiety. α-hydroxy-2',4'-dimethoxy-4-methoxymethoxydihydrochalcone is of interest in the field of natural products chemistry and may have potential applications in pharmaceuticals or as a precursor in the synthesis of other bioactive compounds. Its structure and functional groups suggest that it could exhibit antioxidant, anti-inflammatory, or other therapeutic properties, although further research would be needed to confirm these potential effects.

77412-30-7

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77412-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77412-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77412-30:
(7*7)+(6*7)+(5*4)+(4*1)+(3*2)+(2*3)+(1*0)=127
127 % 10 = 7
So 77412-30-7 is a valid CAS Registry Number.

77412-30-7Relevant academic research and scientific papers

A Novel α-Hydroxydihydrochalcone from the Heartwood of Pterocarpus angolensis D.C.: Absolute Configuration, Synthesis, Photochemical Transformations, and Conversion into α-Methyldeoxybenzoins

Bezuidenhoudt, Barend C. B.,Brandt, E. Vincent,Roux, David G.

, p. 263 - 269 (2007/10/02)

The absolute configuration of (αR)-α,2'-dihydroxy-4,4'-dimethoxydihydrochalcone from the heartwood of Pterocarpus angolensis D.C. is established.Its structure is substantiated by synthesis and by photochemical conversion of its α-O-tosyl derivative into an α-tosyloxymethyldeoxybenzoin and hence to the α-methyldeoxybenzoin analogue.The photochemical step also leads, amongst others, to α-hydroxymethyldeoxybenzoin, β-hydroxydihydrochalcone, and 2-benzylbenzofuran-3-one analogues depending on the conditions the photolysis.

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