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10,10-bis-(4-hydroxybenzyl)-9(10H)-anthracenone is a complex organic compound with the molecular formula C28H20O4. It is characterized by an anthracenone core, which is a derivative of anthracene with a carbonyl group (C=O) at position 9. The compound features two hydroxybenzyl groups attached to the 10th carbon of the anthracenone, with each hydroxybenzyl group containing a hydroxyl (-OH) group and a benzyl (C6H5-CH2-) group. This chemical structure endows the compound with unique properties, such as potential applications in the synthesis of pharmaceuticals, dyes, or other organic materials. The presence of hydroxyl groups also suggests that it may be involved in hydrogen bonding and could have reactivity with other compounds containing active hydrogen or electron-deficient centers.

79769-72-5

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79769-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79769-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79769-72:
(7*7)+(6*9)+(5*7)+(4*6)+(3*9)+(2*7)+(1*2)=205
205 % 10 = 5
So 79769-72-5 is a valid CAS Registry Number.

79769-72-5Relevant academic research and scientific papers

Regioselective Alkylation of Anthrahydroquinone and Anthrone in Water with Quinonemethides and Other Alkylating Agents

Dimmel, Donald R.,Shepard, Donaline

, p. 22 - 29 (2007/10/02)

Antrahydroquinone (AHQ) and anthrone are alkylated in the C10 position by quinonemethides, generated in situ from p-acetoxybenzyl chlorides, to give adducts 13-15, 24, 25, 28, 29, and 32.Aqueous alkylations of AHQ with methyl vinyl ketone, cinnamaldehyde, and benzyl chloride also produces C10-substituted 10-hydroxyanthrones.Simple ketones and aldehydes do not, however, alkylate AHQ in aqueous alkali.

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