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6-amino-3-<2'-carboxy-6'-hydroxyphenylamino>-2,5-dioxo-1,3-cyclohexadiene-1-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112817-49-9

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112817-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112817-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,1 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112817-49:
(8*1)+(7*1)+(6*2)+(5*8)+(4*1)+(3*7)+(2*4)+(1*9)=109
109 % 10 = 9
So 112817-49-9 is a valid CAS Registry Number.

112817-49-9Downstream Products

112817-49-9Relevant academic research and scientific papers

Characterization of a 3-hydroxyanthranilic acid 6-hydroxylase involved in paulomycin biosynthesis

Ding, Yong,Wang, Min,Li, Jine,Li, Pengwei,Guo, Zhenyan,Chen, Yihua

, p. 8 - 14 (2021)

Paulomycins (PAUs) refer to a group of glycosylated antibiotics with attractive antibacterial activities against Gram-positive bacteria. They contain a special ring A moiety that is prone to dehydrate between C-4 and C-5 to a quinone-type form at acidic c

Triphenodioxazine-1,8-dicarboxylic Acid as an Oxidation Product of 3-Hydroxyanthranilic Acid

Hick, Larry A.,Manthey, Michael K.,Truscott, Roger J. W.

, p. 1157 - 1160 (2007/10/02)

The oxidation of 3-hydroxyanthranilic acid (3OHA) 1 by aqueous buffered potassium ferricyanide produces a number of coloured compounds.These include cinnabarinic acid 2 (yellow), a p-quinone dimer 3 (red) and 9-carboxy-2-hydroxy-3H-phenoxazin-3-one 4 (bro

Structural Elucidation and Independent Synthesis of the Radical-Radical Coupling Products of 3-Hydroxyanthranilic acid with Tyrosine and Phenols

Manthey, Michael K.,Pyne, Stephen G.,Truscott, Roger J.W.

, p. 4581 - 4585 (2007/10/02)

The autoxidation of 3-hydroxyanthranilic acid (3OHA) in the presence of tyrosine, p-cresol, or p-ethylphenol gives dibenzopyran-6-one products that arise from the coupling of the radical of 3OHA with that derived from the substituted phenol.As a proo

Autoxidation of 3-Hydroxyanthranilic Acid

Manthey, Michael K.,Pyne, Stephen G.,Truscott, Roger J. W.

, p. 1486 - 1488 (2007/10/02)

3-Hydroxyanthranilic acid in aqueous solution can be autoxidized to yield two different products depending on the pH at which the oxidation is performed.At acidic pH the formation of cinnabarinic acid is favored while at alkaline pHs the major product is

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