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(Benzoyl-hydrazono)-acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111574-79-9

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111574-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111574-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,7 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111574-79:
(8*1)+(7*1)+(6*1)+(5*5)+(4*7)+(3*4)+(2*7)+(1*9)=109
109 % 10 = 9
So 111574-79-9 is a valid CAS Registry Number.

111574-79-9Relevant academic research and scientific papers

Indoline Catalyzed Acylhydrazone/Oxime Condensation under Neutral Aqueous Conditions

Zhou, Yuntao,Piergentili, Irene,Hong, Jennifer,Helm, Michelle P. Van Der,MacChione, Mariano,Li, Yao,Eelkema, Rienk,Luo, Sanzhong

, p. 6035 - 6040 (2020)

Acylhydrazones formation has been widely applied in materials science and biolabeling. However, their sluggish condensation rate under neutral conditions limits its application. Herein, indolines with electron-donating groups are reported as a new catalyst scaffold, which can catalyze acylhydrazone, hydrazone, and oxime formation via an iminium ion intermediate. This new type of catalyst showed up to 15-fold rate enhancement over the traditional anilinecatalyzed reaction at neutral conditions. The identified indoline catalyst was successfully applied in hydrogel formation.

New ampicillin derivatives with glyoxyloylbenzhydrazones as side chains

Heinisch,Hanschke,Willitzer,Mollmann,Tresselt,Stengel,Eckardt,Kleinwachter

, p. 412 - 415 (2007/10/02)

New ampicillin derivatives were synthesized from glyoxylic acid benzhydrazones by reaction with chloroformates via mixed anhydrides and ampicillin. These compounds were tested in an agar diffusion test against six different bacterial strains and also for their stability against β-lactamases. Studies about structure activity relationships have shown, that the activity against different bacterial strains is influenced in different manner by hydrophilic or hydrophobic and electronic properties of substituents.

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