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α-(Methylsulfinylmethyl)-α-phenyl-2-quinolinemethanol is a complex organic compound with the molecular formula C19H19NOS. It is a derivative of quinoline, a heterocyclic aromatic compound, and features a methylsulfinylmethyl group attached to the α-carbon of the phenyl ring. α-(methylsulfinylmethyl)-α-phenyl-2-quinolinemethanol is known for its potential pharmaceutical applications, particularly as an anthelmintic agent, which is used to expel parasitic worms from the body. Its chemical structure endows it with specific biological activities, making it a subject of interest in the field of medicinal chemistry. The compound's unique properties arise from the combination of its quinoline core, phenyl group, and the methylsulfinylmethyl moiety, which together contribute to its therapeutic effects.

16576-29-7

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16576-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16576-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,7 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16576-29:
(7*1)+(6*6)+(5*5)+(4*7)+(3*6)+(2*2)+(1*9)=127
127 % 10 = 7
So 16576-29-7 is a valid CAS Registry Number.

16576-29-7Relevant academic research and scientific papers

Quinoxalines. XXII. Aryl Migration of 2-Aroylquinoxalines to 2-Arylquinoxalines

Higashino, Takeo,Takemoto, Masumi,Tanji, Ken-Ichi,Iijima, Chihoko,Hayashi, Eisaku

, p. 4193 - 4201 (2007/10/02)

The reaction of 2-aroylquinoxalines (1) with sodium hydroxide in dimethyl sulfoxide (DMSO) was found to result in aryl migration, fission of the C2-C=O bond, and addition of DMSO to the C=O group, giving 2-arylquinoxalines (2), quinoxaline (4), aroic acids (5), and α-aryl-α-(methylsulfinylmethyl)-2-quinoxalinemethanols (6).Compounds 6 could be separatedinto two racemates, (αR*,SR*)-6, and (αR*,SS*)-6.In order to establish the generality of the aryl migration, other aroylated aromatic heterocycles were examined. 3-Aroylpyridopyrazines (7) and 1-benzoyl-4-isoquinolinecarbonitrile (10) both underwent similar aryl migration to give 3-arylpyridopyrazines (14) and 1-phenyl-4-isoguinolinecarbonitrile (18), respectively.On the other hand, the reaction of 1-benzoylisoquinoline (9) and 2-benzoilquinoline (11) resulted not in migration, but in the addition of DMSO to give 1-isoquinolinemethanol (16) and 2-quinolinemethanol derivatives (20), respectively.In the case of 1-benzoylphtalazine (8), migration did not occur, but instead 4-benzoyl-1(2H)-phthalazinone (15) was formed.Keywords - 2-aroylquinoxaline; 2-arylquinoxaline; 2-quinoxalinemethanol; aryl migration; racemate; 3-arylpyridopyrazine; 1-isoquinolinemethanol; 2-quinolinemethanol; 1-phenyl-4-isoquinolinecarbonitrile; 4-benzoyl-1(2H)-phthalazinone

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