74020-12-5 Usage
Description
1,6-dimethyl-2-[(Z)-2-(methylsulfanyl)-2-morpholin-4-ylethenyl]quinolinium iodide is a complex organic chemical compound characterized by a quinolinium cation with two methyl groups at positions 1 and 6, and a Z-configured morpholin-4-ylethenyl group attached to the quinolinium ring. 1,6-dimethyl-2-[(Z)-2-(methylsulfanyl)-2-morpholin-4-ylethenyl]quinolinium iodide is associated with an iodide anion, contributing to its unique properties and potential applications in various fields.
Uses
Used in Pharmaceutical Research:
1,6-dimethyl-2-[(Z)-2-(methylsulfanyl)-2-morpholin-4-ylethenyl]quinolinium iodide is utilized as a key component in pharmaceutical research for its potential role in the development of new drugs and treatments. Its structural features make it a valuable asset in organic syntheses and drug design, facilitating the creation of novel therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1,6-dimethyl-2-[(Z)-2-(methylsulfanyl)-2-morpholin-4-ylethenyl]quinolinium iodide serves as a crucial building block for the synthesis of bioactive molecules. Its unique properties allow it to be a versatile component in the design and synthesis of pharmaceuticals with specific therapeutic targets.
Used in the Study of Biological Systems:
1,6-dimethyl-2-[(Z)-2-(methylsulfanyl)-2-morpholin-4-ylethenyl]quinolinium iodide is also employed as a valuable tool in the study of biological systems. Its interaction with biological molecules can provide insights into the mechanisms of action of potential drugs, aiding in the understanding of disease processes and the development of targeted therapies.
Used in Organic Syntheses:
This chemical compound is used as a versatile intermediate in organic syntheses, enabling the production of a wide range of organic compounds with diverse applications. Its reactivity and structural features make it suitable for various synthetic pathways, contributing to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 74020-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,2 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74020-12:
(7*7)+(6*4)+(5*0)+(4*2)+(3*0)+(2*1)+(1*2)=85
85 % 10 = 5
So 74020-12-5 is a valid CAS Registry Number.
74020-12-5Relevant articles and documents
Antileukemic activity of 2-bis(2-methylthio)vinyl-1-methylquinolinium iodides
Foye,Kauffman
, p. 477 - 480 (1980)
Reaction of 1-methylquinolinium-2-dithioacetic acid zwitterions with excess methyl iodide in dimethylformamide gave the corresponding bis(2-methylthio)vinyl derivatives. These compounds were more soluble in both aqueous and organic media than the dithioacetic acid zwitterions but showed comparable antileukemic activity in mice. Reaction with morpholine converted a bis(2-methylthio)vinyl derivative almost quantitatively to the 2-mono(methylthio)-2-morpholino derivative. Leukemia cell culture studies of the 6-methyl derivative showed no effect on cell cycle processes.
