111711-76-3 Usage
Molecular Weight
323.37 g/mol
Pyrrolidin-2-one ring
A five-membered ring with one nitrogen atom and a ketone group (C=O) at the second position.
Ethoxy group
An ethyl group (-CH2CH3) attached to the fifth position of the pyrrolidin-2-one ring.
Sulfonyl group
A group containing a sulfur atom double-bonded to two oxygen atoms (-SO2-) attached to the first position of the pyrrolidin-2-one ring.
3-Acetylphenyl group
A phenyl ring (C6H5) with an acetyl group (-COCH3) attached to the third position, linked to the sulfonyl group.
Ketone (C=O)
Present in the pyrrolidin-2-one ring.
Ether (C-O-C)
Present in the ethoxy group.
Sulfonyl (-SO2-)
Part of the sulfonyl group.
Acetyl (-COCH3)
Present in the 3-acetylphenyl group.
Pharmaceuticals
Due to its unique structure and functional groups, it may have potential as a starting material or intermediate in the synthesis of pharmaceutical compounds.
Organic Synthesis
Its complex structure and various functional groups make it a candidate for use in organic synthesis, potentially leading to the development of new organic compounds.
Reactivity
The ketone group (C=O) in the pyrrolidin-2-one ring can participate in nucleophilic addition and other reactions typical of ketones.
The ether group (C-O-C) in the ethoxy group is generally stable but can undergo cleavage under certain conditions.
The sulfonyl group (-SO2-) is relatively stable and can act as a leaving group in certain reactions.
The acetyl group (-COCH3) in the 3-acetylphenyl group can be hydrolyzed or reduced to form an alcohol or amine, respectively.
Solubility
The compound may be soluble in organic solvents such as dichloromethane, ethyl acetate, or acetone, due to its nonpolar nature and the presence of aromatic and aliphatic groups.
Stability
The compound is likely stable under normal conditions, but it may be sensitive to strong acids, bases, or nucleophiles that could react with its functional groups.
Melting Point
The exact melting point is not provided, but it is expected to be relatively high due to the presence of an aromatic ring and other structural features that promote rigidity and intermolecular interactions.
Boiling Point
The exact boiling point is not provided, but it is expected to be relatively high due to the compound's molecular weight and complexity, which contribute to increased van der Waals forces and other intermolecular interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 111711-76-3 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 111711-76:
(8*1)+(7*1)+(6*1)+(5*7)+(4*1)+(3*1)+(2*7)+(1*6)=83
83 % 10 = 3
So 111711-76-3 is a valid CAS Registry Number.
111711-76-3Relevant articles and documents
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
