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4,6-dibromo-3-hydroxy-2-nitrobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160911-18-2

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160911-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160911-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,9,1 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 160911-18:
(8*1)+(7*6)+(6*0)+(5*9)+(4*1)+(3*1)+(2*1)+(1*8)=112
112 % 10 = 2
So 160911-18-2 is a valid CAS Registry Number.

160911-18-2Relevant academic research and scientific papers

A C2-symmetric, basic Fe(iii) carboxylate complex derived from a novel triptycene-based chelating carboxylate ligand

Li, Yang,Wilson, Justin J.,Do, Loi H.,Apfel, Ulf-Peter,Lippard, Stephen J.

, p. 9272 - 9275 (2012/09/08)

A triptycene-based bis(benzoxazole) diacid ligand H2L2 Ph4 bearing sterically encumbering groups was synthesized. Treatment of H2L2Ph4 with Fe(OTf)3 afforded a C 2-symmetric trinuclear iron

Synthesis and QSAR of substituted 3-hydroxyanthranilic acid derivatives as inhibitors of 3-hydroxyanthranilic acid dioxygenase (3-HAO)

Linderberg, Mats,Hellberg, Sven,Bjoerk, Susanna,Gotthammar, Birgitta,Hoegberg, Thomas,Persson, Kerstin,Schwarcz, Robert,Luthman, Johan,Johansson, Rolf

, p. 729 - 744 (2007/10/03)

Novel 4,5-, 4,6-disubstituted and 4,5,6-trisubstituted 3- hydroxyanthranilic acid derivatives were synthesized and their ability to reduce the production of the excitotoxin quinolinic acid (QUIN) by inhibition of brain 3-hydroxyanthranilic acid dioxygenase (3-HAO) was subsequently investigated. The potency of the compounds to inhibit 3-HAO was assayed in rat brain homogenate, while chemical stability of certain compounds was studied by HPLC. The data were used to generate quantitative structure- activity relationship (QSAR) models for potency of 3-HAO inhibition and compound stability. Compounds with longer half-lives were obtained when the difference between the HOMO and LUMO was increased, while electron withdrawing groups in the 4- and 5-positions increased the potency of 3-HAO inhibition. Selected compounds that showed high potency in vitro were also found to be efficacious inhibitors in vivo after cerebral administration in rats.

NEW COMPOUNDS

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, (2008/06/13)

The present invention relates to novel derivatives of 3-hydroxyanthranilic acid, 3-HANA, of the general formula I wherein R1 and R2 are the same or different and selected from H, alkyl, aryl and arylalkyl; X and Y are the same or different and selected fr

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