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5-Isopropyl-7-methyl-2H-naphtho[1,8-bc]furan-3,4-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57765-65-8

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57765-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57765-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,6 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57765-65:
(7*5)+(6*7)+(5*7)+(4*6)+(3*5)+(2*6)+(1*5)=168
168 % 10 = 8
So 57765-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O3/c1-7(2)12-9-4-8(3)5-11-13(9)10(6-18-11)14(16)15(12)17/h4-5,7,16-17H,6H2,1-3H3

57765-65-8Relevant academic research and scientific papers

The Role of Free Radicals in the Decomposition of the Phytoalexin Desoxyhemigossypol

Stipanovic, Robert D.,Mace, Marshall E.,Bell, Alois A.,Beier, Ross C.

, p. 3189 - 3192 (2007/10/02)

The cotton phytoalexin desoxyhemigossypol (dHG) decomposed rapidly in solution to give hemigossypol (HG).The rate of decomposition was retarded by the reducing agents ascorbic acid, reduced glutathione and cysteine, by the metal chelator diethylenetriaminepentaacetic acid, and by the enzyme catalase.However, the chelator, ethylenediaminetetraacetic acid did not reduce the rate of decomposition and the enzyme superoxide dismutase increased the rate of decomposition.Solutions of the phytoalexin desoxyhemigossypol-6-methyl ether were significantly more stable than were those of dHG.Oxygen-18 from water but not from oxygen gas was incorporated into HG during this decompositon.A hydroperoxynaphthalenone which loses hydrogen peroxide is proposed as an intermediate to explain this observation.The formation of hydrogen peroxide may be involved in the toxicity of this phytoalexin to plant pathogens such as Verticillium dahliae.

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