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"10-{4-nitrophenyl}-7,7-dimethyl-6,7,8,10-tetrahydro-5H-indeno[1,2-b]quinoline-9,11-dione" is a complex organic compound with a molecular formula of C23H19NO4. It is characterized by a tricyclic structure, with a central indole ring fused to a benzene ring, and a quinoline ring fused to the other side. The compound features a 4-nitrophenyl group attached to the 10-position of the indole ring, and two methyl groups at the 7-position. The molecule also contains a 9,11-dione group, indicating the presence of two carbonyl groups at these positions. This chemical is likely to be found in research settings, particularly in the fields of organic chemistry and medicinal chemistry, where it may be studied for its potential applications or properties.

3357-23-1

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3357-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3357-23-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3357-23:
(6*3)+(5*3)+(4*5)+(3*7)+(2*2)+(1*3)=81
81 % 10 = 1
So 3357-23-1 is a valid CAS Registry Number.

3357-23-1Downstream Products

3357-23-1Relevant academic research and scientific papers

Synthesis of indeno-[1,2-: B] -quinoline-9,11(6 H,10 H)-dione and 7,7-dimethyl-10-aryl-7,8-dihydro-5 H -indeno[1,2- b] quinoline-9,11(6 H,10 H)-dione derivatives in presence of heterogeneous Cu/zeolite-Y as a catalyst

Anbhule, Prashant V.,Dhengale, Shankar D.,Kolekar, Govind B.,Rode, Chandrashekhar V.

, p. 2083 - 2093 (2022/02/03)

A simple method for the synthesis of indeno-[1,2-b]-quinoline-9,11-(6H,10H)-dione derivatives and 7,7-dimethyl-10-aryl-7,8-dihydro-5H-indeno[1,2-b]quinoline-9,11(6H,10H)-diones through the reaction of aromatic aldehydes, indan-1,3-dione, dimedone, and p-toluidine/ammonium acetate in the presence of heterogeneous CuO supported on a zeolite-Y catalyst has been investigated in ethanol under reflux conditions. By this method, the reaction time has been reduced, giving an excellent yield of the product. The catalyst was prepared by a hydrothermal method followed by a wet impregnation method. The catalyst had shown Br?nsted acid sites and Lewis acid sites. The used catalyst could be actively recycled with a marginal decrease in yield up to five recycles. The prepared catalyst was characterized by FT-IR, pyridine FT-IR, XRD, SEM, EDS, XPS, TEM, and BET surface area analysis. The synthesized compounds were characterized by FT-IR, 1H NMR, 13C NMR and GC-MS spectroscopy. This journal is

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