105456-99-3 Usage
Quinolinone base
The fundamental structure of the compound, which provides the basis for its chemical properties.
Methoxy group at the 7th position
A methoxy (-OCH3) group attached to the quinolinone base at the 7th position, which can influence the compound's reactivity and solubility.
Ethynyl-phenylamino group at the 3rd position
An ethynyl (-C≡C-) group connected to a phenylamino (-NH-C6H5) group at the 3rd position, which can affect the compound's chemical reactivity and physical properties.
Morpholine ring substitution at the 4th position
A morpholine (C4H8N2O2) ring attached to the quinolinone base at the 4th position, which can impact the compound's solubility, stability, and biological activity.
Potential medicinal properties
The unique structure and chemical properties of the compound may make it suitable for pharmaceutical applications, but further research is needed to fully understand its biological effects and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 105456-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,5 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105456-99:
(8*1)+(7*0)+(6*5)+(5*4)+(4*5)+(3*6)+(2*9)+(1*9)=123
123 % 10 = 3
So 105456-99-3 is a valid CAS Registry Number.
105456-99-3Relevant academic research and scientific papers
Polyynes, 9. - Reactions of Butadiynediamines and of One Butadiynamine with Aryl Isocyanates
Barz, Michael,Feustel, Michael,Himbert, Gerhard,Maas, Gerhard
, p. 221 - 226 (2007/10/02)
The butadiynamine 6 and the butadiynediamines 5a-c react with the aryl isocyanates 7a-c and 8 by cyclization to give the 2-quinolone derivatives 10 and 11.The representatives of 10 and 11 bearing an aminoethinyl moiety formed from diynamines 5 cyclize on
