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ethyl 7-methyl-4-phenylquinoline-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1341220-91-4

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1341220-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1341220-91-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,1,2,2 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1341220-91:
(9*1)+(8*3)+(7*4)+(6*1)+(5*2)+(4*2)+(3*0)+(2*9)+(1*1)=104
104 % 10 = 4
So 1341220-91-4 is a valid CAS Registry Number.

1341220-91-4Downstream Products

1341220-91-4Relevant academic research and scientific papers

Synthesis and anti-toxoplasmosis activity of 4-arylquinoline-2-carboxylate derivatives

McNulty, James,Vemula, Ramesh,Bordon, Claudia,Yolken, Robert,Jones-Brando, Lorraine

supporting information, p. 255 - 260 (2014/01/06)

A one-step synthesis of 4-arylquinoline-2-carboxylates along with their antiprotozoal activity against the pathogenic parasite Toxoplasma gondii is reported. Mechanistic insights into the role of Lewis acid (silver triflate) versus Bronsted acid (triflic

Iron-catalyzed oxidative tandem reactions with TEMPO oxoammonium salts: Synthesis of dihydroquinazolines and quinolines

Rohlmann, Renate,Stopka, Tobias,Richter, Heinrich,Garcia Mancheno, Olga

, p. 6050 - 6064 (2013/07/26)

A straightforward iron-catalyzed divergent oxidative tandem synthesis of dihydroquinazolines and quinolines from N-alkylanilines using a TEMPO oxoammonium salt as a mild and nontoxic oxidant has been developed. Fe(OTf) 2 was the Lewis acid cata

TEMPO oxoammonium salt-mediated dehydrogenative Povarov/oxidation tandem reaction of N-alkyl anilines

Richter, Heinrich,Garcia Mancheno, Olga

supporting information; experimental part, p. 6066 - 6069 (2012/01/13)

The synthesis of a variety of substituted quinolines from N-alkyl anilines by a one-pot dehydrogenative Povarov/oxidation tandem reaction with mono- and 1,2-disubstituted aryl and alkyl olefins was developed. A simple protocol using cheap and benign iron(

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