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Trans-3',4'-dimethoxy-4-hydroxy-6-methylflavan is a naturally occurring flavonoid compound characterized by its unique chemical structure. Flavonoids are a diverse group of plant-derived polyphenolic compounds known for their antioxidant properties and potential health benefits. This specific flavan, with the molecular formula C18H18O6, features a flavan skeleton with a 6-methyl group, a hydroxyl group at the 4-position, and two methoxy groups at the 3' and 4' positions. These substitutions contribute to its distinct chemical properties and potential biological activities. The trans configuration of the compound refers to the arrangement of the double bond in the molecule, which can influence its reactivity and stability. Research on flavonoids like this one often focuses on their antioxidant, anti-inflammatory, and anticancer effects, although more studies are needed to fully understand their mechanisms of action and therapeutic potential.

2181-18-2

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2181-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2181-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,8 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2181-18:
(6*2)+(5*1)+(4*8)+(3*1)+(2*1)+(1*8)=62
62 % 10 = 2
So 2181-18-2 is a valid CAS Registry Number.

2181-18-2Relevant academic research and scientific papers

STEREOSELECTIVITY AT BENZYLIC CARBON. FLAVANOIDS-V. SYNTHESIS OF TRANS-4-ACETAMIDOFLAVANS

Hirwe, A.,Marathe, K. G.,Mohorkar, S. S.,Ramdas, K.,Singh, C. B.

, p. 1539 - 1546 (2007/10/02)

Some reactions of 4-substituted flavans have been studied. 4-Chloro/bromo derivatives react under neutral conditions with phthalimide and acetonitrile leading to displacement of axial halogen by nitrogen with inversion.In contrast, irrespective of the ste

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