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3-Hydroxy-1-methylxanthone is a naturally occurring organic compound belonging to the xanthone family, characterized by a unique chemical structure consisting of a xanthone core with a hydroxyl group at the 3-position and a methyl group at the 1-position. This yellow crystalline substance is found in various plants and has been reported to possess potential biological activities, such as antioxidant and anti-inflammatory properties. Its chemical formula is C13H10O3, and it has a molecular weight of 214.22 g/mol. The compound is known for its UV-absorbing properties, making it a potential candidate for use in sunscreens and other cosmetic applications. Additionally, 3-hydroxy-1-methylxanthone has been studied for its potential role in the treatment of various diseases due to its pharmacological properties.

3875-66-9

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3875-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3875-66-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3875-66:
(6*3)+(5*8)+(4*7)+(3*5)+(2*6)+(1*6)=119
119 % 10 = 9
So 3875-66-9 is a valid CAS Registry Number.

3875-66-9Downstream Products

3875-66-9Relevant academic research and scientific papers

Studies in Synthesis of Xanthone Derivatives: Part III+ - A New One-step Synthesis of Xanthones

Patolia, Ravji J.,Trivedi, K. N.

, p. 444 - 447 (2007/10/02)

Ethyl salicylate condenses with different phenols in refluxing diphenyl ether to give various xanthones in good yields.In the case of resorcinol, hydroquinone, catechol and 3,4-xylenol corresponding phenyl salicylate derivatives are also obtained.Condensation with hydroxycoumarins affords pyranoxanthones, which can not be prepared by the Pechmann condensation of hydroxyxanthones.The structures of the intermediates and final products are established by spectral data (IR, PMR and 13C NMR).

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