24476-55-9 Usage
Description
4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile is a chemical compound with the molecular formula C21H20N2O2S. It is a piperidine derivative that features a phenyl group, a p-tolylsulphonyl group, and a carbonitrile group. 4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile is likely to have various potential applications in medicinal chemistry, particularly as a potential drug or intermediate in the synthesis of pharmaceuticals. The presence of the piperidine ring and the sulphonyl group suggests that it may exhibit biological activity, making it a compound of interest in the development of therapeutically useful compounds. Further research and study are required to fully understand the properties and potential uses of 4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile.
Uses
Used in Pharmaceutical Industry:
4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile is used as a potential drug candidate for the development of new therapeutic agents. Its unique structure, including the piperidine ring and sulphonyl group, may contribute to its biological activity and potential efficacy in treating various diseases.
Used in Medicinal Chemistry Research:
4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile serves as an intermediate in the synthesis of pharmaceuticals. Its chemical properties and reactivity can be exploited to create new compounds with potential therapeutic applications.
Used in Drug Discovery:
4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile is utilized in drug discovery processes to identify novel compounds with potential therapeutic effects. Its unique structural features may provide a starting point for the design and optimization of new drugs targeting specific biological pathways or receptors.
Used in Chemical Synthesis:
4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile can be employed as a building block in the synthesis of more complex organic molecules. Its versatile functional groups, such as the carbonitrile and sulphonyl groups, can be used in various chemical reactions to form new compounds with potential applications in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 24476-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,7 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24476-55:
(7*2)+(6*4)+(5*4)+(4*7)+(3*6)+(2*5)+(1*5)=119
119 % 10 = 9
So 24476-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H20N2O2S/c1-16-7-9-18(10-8-16)24(22,23)21-13-11-19(15-20,12-14-21)17-5-3-2-4-6-17/h2-10H,11-14H2,1H3
24476-55-9Relevant articles and documents
MELANOCORTIN RECEPTOR ANTAGONIST COMPOUNDS, PROCESS FOR PREPARING THEM AND USE THEREOF IN HUMAN MEDICINE AND COSMETICS
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Page/Page column 25, (2010/06/11)
The present invention relates to novel melanocortin receptor antagonist compounds corresponding to the general formula (I) below, to compositions containing them, to the process for preparing them and to their use in pharmaceutical or cosmetic compositions.
Synthesis and antinociceptive activity of ring substituted N-[(2-phenyl-2-hydroxy)ethyl]-4-phenyl-4-carboethoxypiperidines
Al-Rashood,Madani,Ginawi,Ashraf,El-Obeid
, p. 1242 - 1245 (2007/10/02)
A series of phenyl substituted N-[(2-phenyl-2-hydroxy)ethyl]-4-phenyl-4-carboethoxylpiperidine were synthesized and their antinociceptive activity tested in mice and compared with morphine sulphate. All compounds demonstrated antinociceptive activity in both the hot plate and the writhing tests. The studies showed that the antinociceptive activity is dependable on both the nature and the position of the substituent on the phenyl ring. Antagonism study with naloxone, suggests possible interaction of the new compounds with the opioid receptors.