24476-55-9 Usage
General Description
4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile is a chemical compound with the molecular formula C21H20N2O2S. It is a piperidine derivative that contains 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 have biological activity and could be 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.
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.