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α,4-Dihydroxy-2',4'-dimethoxydihydrochalcone is a naturally occurring chemical compound belonging to the class of dihydrochalcones, which are derived from flavonoids. This specific compound is characterized by the presence of two hydroxyl groups at the α and 4 positions, and two methoxy groups at the 2' and 4' positions. It is known for its potential antioxidant and anti-inflammatory properties, which are being studied for their potential health benefits. The compound is found in certain plants and has been the subject of research in the field of natural products chemistry and pharmacology. Its structure and functional groups contribute to its biological activities, making it a subject of interest for further exploration in medicinal and dietary applications.

77412-36-3

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77412-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77412-36-3 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 77412-36:
(7*7)+(6*7)+(5*4)+(4*1)+(3*2)+(2*3)+(1*6)=133
133 % 10 = 3
So 77412-36-3 is a valid CAS Registry Number.

77412-36-3Downstream Products

77412-36-3Relevant 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 (1981)

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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