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4-(7-chloro-4-quinolinylamino)phenol 1-oxide, also known as 4-(7-chloroquinolin-4-yl)phenol 1-oxide, is a chemical compound with the molecular formula C15H10ClNO2. It is a derivative of phenol, featuring a 7-chloro-4-quinolinylamine group attached to the 4-position of the phenol ring. 4-(7-chloro-4-quinolinylamino)phenol 1-oxide is an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of antimalarial and anticancer drugs. Its chemical structure allows for the formation of hydrogen bonds and other interactions, which contribute to its potential therapeutic properties. The presence of the chlorine atom in the 7-position of the quinoline ring can influence the compound's reactivity and biological activity.

1090-30-8

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1090-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1090-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1090-30:
(6*1)+(5*0)+(4*9)+(3*0)+(2*3)+(1*0)=48
48 % 10 = 8
So 1090-30-8 is a valid CAS Registry Number.

1090-30-8Relevant academic research and scientific papers

Anticholinesterase activity of 4-aminoquinolines related to amodiaquine and their respective N-oxides

Go,Ngiam,Lim

, p. 81 - 85 (2007/10/02)

The inhibitory activities of a series of substituted 4-aminoquinolines related to the antimalarial agent amodiaquine and their respective N-oxides toward acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) have been determined and discussed in terms of their proposed mode of interaction with the enzyme surface. A marked difference was noted in the AChE and BChE inhibitory potencies of these compounds. The strong anti-AChE activity of amodiaquine has been explained by a specific two-point interaction with the anionic site and acidic group of AChE. However, such an interaction appears to be absent in the case of the amodiaquine inhibition of BChE, suggesting differences in the ability of the enzymes to accommodate similar inhibitory molecules.

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