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N-(2-iodophenyl)furan-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

860263-13-4

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860263-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 860263-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,2,6 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 860263-13:
(8*8)+(7*6)+(6*0)+(5*2)+(4*6)+(3*3)+(2*1)+(1*3)=154
154 % 10 = 4
So 860263-13-4 is a valid CAS Registry Number.

860263-13-4Relevant academic research and scientific papers

Palladium-mediated intramolecular biaryl coupling reaction: Convenient preparation of furoquinolinone derivatives

Abe, Hitoshi,Kamimura, Mayu,Komatsu, Yoshinori,Horino, Yoshikazu

, p. 1332 - 1342 (2015)

Furo[2,3-c ] or furo[3,2-c ]quinolinone derivatives were prepared via the intramolecular biaryl coupling reaction of 2-furoylanilides or 3-furoylanilides using a palladium catalyst.

Synthesis of 5-methylfuro[3,2-c]quinolin-4(5H)-one via palladium-catalysed cyclisation of N-(2-iodophenyl)-N-methyl-3-furamide

Lindahl, Karl-Fredrik,Carroll, Anthony,Quinn, Ronald J.,Ripper, Justin A.

, p. 7493 - 7495 (2007/10/03)

A new synthesis of the furo[3,2-c]quinolin-4(5H)-one heterocycle has been developed using a palladium-catalysed cyclisation of N-(2-iodophenyl)-N-methyl-3-furamide. By varying the catalyst, base and solvent, the yield of the cyclisation was optimised. It

Synthesis of tricyclic quinolones and naphthyridones by intramolecular heck cyclization of functionalized electron-rich heterocycles

Beccalli, Egle M.,Broggini, Gianluigi,Martinelli, Michela,Paladino, Giuseppe,Zoni, Caterina

, p. 2091 - 2096 (2007/10/03)

Starting from commercially available pyrrole- and thiophene-2-carboxylic acids 1 or thiophene- and furan-3-carboxylic acids 6, we report the synthesis of tricyclic fused quinolone and naphthyridone derivatives, in only three steps, by an intramolecular He

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