142841-84-7 Usage
Uses
Used in Organic Synthesis:
Used in Material Science:
The highly conjugated system and electron-rich nature of this compound may make it suitable for use in the development of advanced materials with tailored electronic, optical, or magnetic properties. It could potentially be incorporated into the design of organic semiconductors, conductive polymers, or other materials with specific functionalities.
Used in Drug Design:
Used in Chemical Research:
5''-(2-methyl-8-quinolinyl)-5',5'''-diphenyl-'s intricate structure and potential for modification make it an interesting subject for chemical research. It could be used to study the effects of structural variations on the properties and reactivity of organic molecules, contributing to the broader understanding of organic chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 142841-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,8,4 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 142841-84:
(8*1)+(7*4)+(6*2)+(5*8)+(4*4)+(3*1)+(2*8)+(1*4)=127
127 % 10 = 7
So 142841-84-7 is a valid CAS Registry Number.
142841-84-7Relevant articles and documents
Receptors for Oxo Acids: Effects of Intra-Ion-Pair Hydrogen Bonding on Acid-Base Equilibria
Manabe, Kei,Okamura, Kimio,Date, Tadamasa,Koga, Kenji
, p. 6692 - 6700 (2007/10/02)
Receptor molecules 1-3 containing a quinoline unit and hydroxyl groups were synthesized, and their properties in salt formation with oxo acids such as p-toluenesulfonic acid (TsOH) and methyl phenylphosphonate (MPP) were studied by using 1H NMR spectroscopy.In CDCl3 solution the salt formation of the receptors with TsOH or MPP is enhanced by hydrogen bonds between the hydroxyl groups and the counteranion.The salt-formation enhancement of 1 over 2 suggests the presence of multiple interactions.The X-ray structure of 1*MPP*(acetone)2 confirms that threehydrogen-bonding interactions stabilize the salt.In the salt formation of 5-(dimethylamino)quinoline derivative 3, the hydroxyl groups also affect the relative basicity of the basic nitrogens in 3.The results described here emphasize that acid-base equilibria in apolar solvents are significantly affected by intra-ion-pair hydrogen bonding (i.e., hydrogen bonding within a contact ion pair).