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2(1H)-Quinolinone, 4-[(phenylmethyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80356-47-4

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80356-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80356-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,5 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80356-47:
(7*8)+(6*0)+(5*3)+(4*5)+(3*6)+(2*4)+(1*7)=124
124 % 10 = 4
So 80356-47-4 is a valid CAS Registry Number.

80356-47-4Relevant academic research and scientific papers

4-Hydro-2-quinolones. 192. *relationship of xy structure and analgesic activity of 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acids and their derivatives

Ukrainets,Mospanova,Davidenko,Shishkina

experimental part, p. 1371 - 1379 (2011/10/18)

Some 4-N-R-2-Oxo-1,2-dihydroquinoline-3-carboxylic acids and their derivatives were synthesized as close structural analogs of the highly-active analgesic 4-benzylamino-2-oxo-1,2-dihydroquinoline-carboxylic acid. Pharmacological testing showed that manife

COMPOUNDS, COMPOSITIONS AND METHODS

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Page/Page column 73-74; 35, (2010/11/24)

Compounds useful for treating cellular proliferative diseases and disorders by modulating the activity of KSP are disclosed.

4-Hydroxyquinol-2-ones. 87. Unusual synthesis of 1-R-4-hydroxy-1-oxo-1,2- dihydroquinoline-3-carboxylic acid pyridylamides

Ukrainets,Sidorenko,Slobodzyan,Rybakov,Chernyshev

, p. 1158 - 1166 (2007/10/03)

4-Chloro-2-oxo-1,2-dihydroquinoline-3-carboxylic acids and their esters react with aminopyridines in refluxing DMF to give the corresponding 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid pyridylamides. Their structures were proved by 1

Methods for the Synthesis of 4-Azido-2(1H)-quinolones

Stadlbauer, Wolfgang

, p. 1305 - 1324 (2007/10/02)

4-Hydroxy-2-quinolones 1 are generally found to be converted to the 4-azidocompounds 3 via the 4-chloroquinolones 2, the 4-tosyloxyquinolones 6, or the 4-aminoquinolones 4, respectively.Choice of the reaction conditions and yields depend on the substituen

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