84255-02-7 Usage
Uses
Used in Pharmaceutical Industry:
4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carboxylic acid is used as a potential starting material for the synthesis of new medications due to its complex structure and the presence of functional groups that can be further modified or utilized in chemical reactions.
Used in Medicinal Chemistry Research:
As a compound with a unique structure, 4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carboxylic acid is used in research for the development of novel therapeutic agents, where its properties can be explored and optimized for specific medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 84255-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,5 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84255-02:
(7*8)+(6*4)+(5*2)+(4*5)+(3*5)+(2*0)+(1*2)=127
127 % 10 = 7
So 84255-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H21NO4S/c1-15-7-9-17(10-8-15)25(23,24)20-13-11-19(12-14-20,18(21)22)16-5-3-2-4-6-16/h2-10H,11-14H2,1H3,(H,21,22)
84255-02-7Relevant academic research and scientific papers
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.
