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3-[5-(2-nitrophenyl)furan-2-yl]benzo[f]quinoline-1-carboxylic acid is a complex organic compound with the molecular formula C23H13N3O5. It is characterized by a benzo[f]quinoline core, which is a fused ring system consisting of a benzene ring and a quinoline ring. The molecule features a furan-2-yl group at position 5, which is substituted with a 2-nitrophenyl group. 3-[5-(2-nitrophenyl)furan-2-yl]benzo[f]quinoline-1-carboxylic acid has a carboxylic acid functional group at the 1-position of the benzo[f]quinoline ring, which can participate in various chemical reactions due to its acidic properties. The presence of the nitro group on the phenyl ring introduces a strong electron-withdrawing effect, which can influence the reactivity and physical properties of the molecule. This chemical structure is of interest in the field of medicinal chemistry, potentially for its biological activities or as a precursor in the synthesis of other compounds.

6255-38-5

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6255-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6255-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6255-38:
(6*6)+(5*2)+(4*5)+(3*5)+(2*3)+(1*8)=95
95 % 10 = 5
So 6255-38-5 is a valid CAS Registry Number.

6255-38-5Downstream Products

6255-38-5Relevant academic research and scientific papers

Exploring the reactivity of tungsten bis(imido) dimethyl complexes with methyl aluminium reagents: Implications for ethylene dimerization

Wright, William R. H.,Batsanov, Andrei S.,Howard, Judith A. K.,Tooze, Robert P.,Hanton, Martin J.,Dyer, Philip W.

experimental part, p. 7038 - 7045 (2010/09/06)

The reaction of [WCl2(NAr)2(DME)] (1) with excess Me3Al affords the dimethyl complex [WMe2(N{Ar}AlMe 2{μ-Cl})(NAr)] (2), which on treatment with THF or MeAlCl 2 yields [WMe2(NAr)2(THF)] (3) and [WMe 2(N{Ar}AlMe(Cl){μ-Cl})(NAr)] (5), respectively. Complex 3 is unstable in solution dissociating to form [WMe2(NAr)2] (4) that may be isolated as an adduct with PMe3, [WMe 2(NAr)2(PMe3)] (6). While complex 2 is inert towards ethylene, complex 3 reacts rapidly to afford a mixture of methane and but-1-ene (1:4). Neither complex 2 nor 3 react with propylene. Reaction of 3 with a C2H4/C2D4 (1:1) affords a mixture of isotopomers that is consistent with complete isotopic scrambling. The structures of complexes 1, 2, and 3 have been determined by X-ray diffraction. The Royal Society of Chemistry 2010.

Reaction of n-Butenes on Nickel Films

Ledoux, Marc J.,Gault, Francois G.,Boughy, Alain,Roussy, Georges

, p. 1547 - 1561 (2007/10/02)

The reactions on nickel films of all three butenes (exchange, double-bond migration and cis-trans isomerization) were investigated at 0-20 deg C in the presence of C3D6 and at -84 deg C in the presence of D2.Analyses of the reaction products were made by mass spectrometry and microwave spectroscopy.The hyperfine distributions of the and but-1-enes obtained by exchange suggest a vinylic-type dissociative mechanism (Farkas mechanism).Cis-trans isomerization takes place either by an associative Horiuti-Polyani mechanism or by a direct process without deuterium incorporation.Three reaction mechanisms account for double-bond migration: intramolecular hydrogen shift, associative mechanism and allylic mechanism.The latter involves a number of interconversions between ?-olefinic and ?-allylic adsorbed species and yields multideuterated molecules.The above reaction mechanisms may be classified into three groups, according to their activation energies, and are believed to occur on three different types of sites with different coordination numbers.This view is supported by the changes in reaction mechanisms that result from film modification.

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