111711-72-9 Usage
Molecular structure
The compound has a complex molecular structure consisting of a pyrrolidin-2-one ring, an ethoxy group, and a sulfonyl group with a 2,6-dimethylphenyl substituent.
Ethoxy group
The presence of an ethoxy group attached to the fifth position of the pyrrolidin-2-one ring may enhance the compound's solubility in organic solvents.
Sulfonyl group
The sulfonyl group attached to the first position of the pyrrolidin-2-one ring contains a 2,6-dimethylphenyl substituent, which could contribute to the compound's potential pharmaceutical applications.
Potential pharmaceutical applications
Due to its unique structure, 1-[(2,6-dimethylphenyl)sulfonyl]-5-ethoxypyrrolidin-2-one may be suitable for binding to specific biological targets, making it a candidate for pharmaceutical development.
Sulfamethizole analog
The compound shares structural similarities with the antimicrobial drug sulfamethizole, suggesting that it may have potential as a sulfonamide with antimicrobial and antiviral properties.
Industrial applications
The compound's solubility in organic solvents, due to the presence of the ethoxy group, could make it useful in chemical synthesis and other industrial applications.
Chemical synthesis
The compound's unique structure and functional groups may allow for further chemical modifications and the development of new derivatives with potential applications in various fields.
Research and development
Further research and development are needed to fully understand the compound's properties, potential applications, and any possible side effects or limitations.
Check Digit Verification of cas no
The CAS Registry Mumber 111711-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,7,1 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111711-72:
(8*1)+(7*1)+(6*1)+(5*7)+(4*1)+(3*1)+(2*7)+(1*2)=79
79 % 10 = 9
So 111711-72-9 is a valid CAS Registry Number.
111711-72-9Relevant academic research and scientific papers
Amnesia-reversal activity of a series of 5-alkoxy-1-arylsulfonyl-2-pyrrolidinones
Toja, E,Gorini, C,Zirotti, C,Barzaghi, F,Galliani, G
, p. 403 - 413 (2007/10/02)
A series of 5-alkoxy-1-arylsulfonyl-2-pyrrolidinones were prepared by condensation of arylsulfonyl chlorides with 5-alkoxy-2-pyrrolidinones.Most compounds reversed electroconvulsive shock-induced amnesia in mice, showing the typical inverted U-shaped dose
