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Benzoic acid, 2,2'-[(1,3-dioxo-1,3-propanediyl)diimino]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77317-57-8

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77317-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77317-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,1 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77317-57:
(7*7)+(6*7)+(5*3)+(4*1)+(3*7)+(2*5)+(1*7)=148
148 % 10 = 8
So 77317-57-8 is a valid CAS Registry Number.

77317-57-8Relevant academic research and scientific papers

4-Hydroxy-2-quinolones. 112. Reaction of 2-ethoxycarbonylmethyl-4H-3,1- benzoxazin-4-one with active methylene compounds

Ukrainets,Sidorenko,Gorokhova,Slobodzyan

, p. 63 - 66 (2007)

The reaction of 2-ethoxycarbonylmethyl-4H-3,1-benzoxazin-4-one with malononitrile in dry pyridine leads to 1-hydroxy-3,6-dioxo-4,6-dihydro-3H- pyrimido[1,2-a]quinoline-5-carbonitrile. Acetoacetic and cyanoacetic esters under analogous conditions form anil

Ethyl Esters of Malonanilic Acids. Synthesis and Pyrolysis

Ukrainets, Igor V.,Bezugly, Peter A.,Treskach, Vladimir I.,Taran, Svetlana G.,Gorokhova, Olga V.

, p. 10331 - 10338 (2007/10/02)

The pyrolysis under 170-220 deg C or boiling in DMF of malonanilic acids ethyl esters (2) is accompanied by formation of malonic acids symmetric dianilides (7) with high yields.A possible mechanism for this transformation has been suggested.

2-CARBETHOXY-4H-3,1-BENZOXAZIN-4-ONE. 1. SYNTHESIS AND REACTION MECHANISM OF FORMATION

Ukrainets, I. V.,Bezuglyi, P. A.,Treskach, V. I.,Slobodzyan, S. V.

, p. 903 - 907 (2007/10/02)

The possibility was examined of using various condensing agents in the intramolecular cyclization reaction of ethyl ester of 2-carbomalonanilic acid into 2-carboethoxymethyl-4H-3,1-benzoxazin-4-one.It was found that the optimal reagent is dicyclohexylcarbodiimide.By using NMR spectroscopy and deutero-exchange it was shown that the cyclization proceeds with the participation of the hydroxyl group of the carboxyl and a proton of the amide function.

ACYLATION OF ORTHO(PARA)-SUBSTITUTED AROMATIC AMINES BY MALONIC ACID DERIVATIVES

Bezuglyi, P. A.,Treskach, V. I.,Ukrainets, I. V.,Grinenko, V. V.,Bevz, N. Yu.

, p. 1233 - 1236 (2007/10/02)

The reaction of diethyl malonate with primary ortho(para)-substituted arylamines leads to the formation of ethyl malonanilates or symmetrical malonanilides, depending on the temperature and on the nucleophilic characteristics of the amines.

[(1,3-dioxo-1,3-propanediyl)diimino)]bisbenzoic acid derivatives

-

, (2008/06/13)

Compounds of the general formula: STR1 wherein A and B are both hydrogen, or one of A and B is a group (G) of the formula: STR2 and the other is a group R5 wherein R1 is an aryl group or a heterocyclic group, both of them being optio

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