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Propanoic acid, 2-[2-(2-nitrophenyl)hydrazinylidene]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

292853-66-8

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292853-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292853-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,8,5 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 292853-66:
(8*2)+(7*9)+(6*2)+(5*8)+(4*5)+(3*3)+(2*6)+(1*6)=178
178 % 10 = 8
So 292853-66-8 is a valid CAS Registry Number.

292853-66-8Relevant academic research and scientific papers

N-acyl sulfamide FBPase inhibitor, preparation method thereof, drug composition and application

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Paragraph 2633; 2636-2638, (2017/09/08)

The invention discloses an N-acryl sulfamide FBPase inhibitor of a novel structure, and a preparation method thereof, a drug composition and an application, and particularly relates to an N-acryl sulfamide FBPase inhibitor shown in the formula I, a salt thereof for medicine, a preparation method, a composition comprising one or more compounds, an application of the compound in preparing the FBPase inhibitor or a drug for treating FBPase-related diseases, and an application in preparing a drug for preventing and/or treating diabetes. The formula is shown in the description.

Design, synthesis and biological evaluation of 7-nitro-1H-indole-2- carboxylic acid derivatives as allosteric inhibitors of fructose-1,6- bisphosphatase

Bie, Jianbo,Liu, Shuainan,Zhou, Jie,Xu, Bailing,Shen, Zhufang

, p. 1850 - 1862 (2014/03/21)

A series of novel indole derivatives was synthesized as inhibitors of fructose-1,6-bisphosphatase (FBPase). Extensive structure-activity relationships were conducted and led to a potent FBPase inhibitor 3.9 with an IC50 of 0.99 μM. The binding mode of this series of indoles was predicted using CDOCKER algorithm. The results of this research will shed light on the further design and optimization of novel small molecules as FBPase inhibitors.

A simple and efficient synthesis of ethyl 1-Aryl-4-formyl-1H-pyrazole-3- carboxylates

Matiychuk, Vasyl S.,Potopnyk, Mykhaylo A.,Obushak, Mykola D.

, p. E43-E47 (2013/06/04)

A new simple and convenient method of synthesis of ethyl 1-aryl-4-formyl-1H-pyrazole-3-carboxylates from aromatic amines via diazonium salts has been developed. Hydrolysis and hydrazinolyization of these compounds has been investigated.

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