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ethyl 1,4,5,6,7,8‐hexahydro‐4‐(2,4‐dimethoxyphenyl)‐2,7,7‐trimethyl‐5‐oxoquinoline‐3‐carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

292853-34-0

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292853-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292853-34-0 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, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 292853-34:
(8*2)+(7*9)+(6*2)+(5*8)+(4*5)+(3*3)+(2*3)+(1*4)=170
170 % 10 = 0
So 292853-34-0 is a valid CAS Registry Number.

292853-34-0Downstream Products

292853-34-0Relevant academic research and scientific papers

5-Pyrrolidin-2-yltetrazole-promoted one-pot hantzsch polyhydroquinoline synthesis using NH4HCO3 as nitrogen source

Su, Weike,Li, Jia,Li, Jianjun

, p. 860 - 863 (2008)

A straightforward and green synthesis of polyhydroquinoline derivatives was reported via a four-component coupling reaction of aldehydes, dimedone, active methylene compounds, and ammonium bicarbonate in the presence of 5-pyrrolidin-2-yltetrazole under solvent-free conditions. The method offers several advantages including high yields, an environmental friendly procedure, a short reaction time, and easy isolation of products.

Facile and efficient protocols for C–C and C–N bond formation reactions using a superparamagnetic palladium complex as reusable catalyst

Karimi Zarchi, Mohammad Ali,Darbandizadeh Mohammad Abadi, Seyed Shahab Addin

, p. 2605 - 2639 (2019/02/13)

Abstract: Facile and efficient protocols for some multicomponent coupling reactions such as the Suzuki reaction and synthesis of polyhydroquinoline and 2,3-dihydroquinazoline-4-(1H)-one derivatives using a superparamagnetic palladium complex as catalyst have been developed. Graphical abstract: [Figure not available: see fulltext.].

Sucrose chelated auto combustion synthesis of BiFeO3 nanoparticles: Magnetically recoverable catalyst for the one-pot synthesis of polyhydroquinoline

Singh, Harminder,Garg, Nidhi,Arora, Priya,Rajput, Jaspreet Kaur,Jigyasa

, (2018/04/26)

Sucrose chelated Bismuth ferrite (BiFeO3) nanoparticles as a novel heterogeneous catalyst was synthesized by an auto combustion route. Different calcination temperatures (150?°C, 450?°C, 550?°C, 650?°C, 750?°C and 850?°C) have been employed to obtain single phased BiFeO3 nanoparticles. The perovskite structure formation and disappearance of organic phase (sucrose) was obtained by Fourier transform infrared spectroscopy (FT-IR). Phase determination and structural characterization was carried out by powder X-ray diffraction (XRD). The magnetic properties were analyzed by vibrating sample magnetometer (VSM) whereas surface area/pore volume was obtained by Brunauer–Emmett–Teller (BET). Transmission electron microscope (TEM) analyzed the particles size and morphology. Thermal stability was investigated by thermogravimetric analysis (TGA) and determination of constituent elements was carried out by X-ray Photo-Electron Spectroscopy (XPS). Raman spectroscopy confirmed the perovskite structure of the synthesized materials. The BiFeO3 nanoparticles so obtained were employed as heterogeneous catalyst for the synthesis of polyhydroquinoline derivatives. All the polyhydroquinoline derivatives were characterized by Fourier transform infrared spectroscopy (FT-IR) and Nuclear magnetic resonance spectroscopy (1H NMR). For the very first time ever we have used BiFeO3 as a recyclable magnetic nanocatalyst in the one-pot four component cyclization reaction of benzaldehyde, ethylacetoacetate/methylacetoacetate, dimedone/cyclohexane-1,3-dione, and ammonium acetate for the synthesis of polyhydroquinoline derivatives without solvent under refluxing conditions to provide excellent yields of products. BiFeO3 nanocatalyst (without any functionalization/surface coatings) shows easy magnetic separation, recyclability, reusability along with excellent yield of polyhydroquinoline derivatives in an economic and benign way.

RETRACTED ARTICLE: One-pot synthesis of Hantzsch dihydropyridines using a highly efficient and stable PdRuNi@GO catalyst

Demirci, Tuna,?elik, Betül,Yildiz, Yunus,Eri?, Sinan,Arslan, Mustafa,Sen, Fatih,Kilbas, Benan

, p. 76948 - 76956 (2016/08/30)

Addressed herein, highly monodispersed PdRuNi nanoparticles furnished with graphene oxide (PdRuNi@GO NPs) were prepared as novel, stable, efficient and exceptionally reusable heterogeneous catalysts for 1,4-dihydropyridine synthesis via multicomponent con

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