30256-73-6 Usage
Description
1-(1H-indol-3-yl)-2-(piperidin-1-yl)ethanone is a chemical compound featuring an indole group and a piperidine group connected by an ethanone linker. It is recognized for its potential pharmacological activity and is considered a promising drug candidate for various therapeutic applications due to its demonstrated anti-inflammatory, anticonvulsant, and antitumor properties in preclinical studies. 1-(1H-indol-3-yl)-2-(piperidin-1-yl)ethanone's unique structure and potential biological activities make it an intriguing subject for further research and development within the medicinal chemistry field.
Uses
Used in Pharmaceutical Industry:
1-(1H-indol-3-yl)-2-(piperidin-1-yl)ethanone is used as a potential therapeutic agent for its anti-inflammatory properties, aiming to alleviate inflammation-related conditions and diseases.
1-(1H-indol-3-yl)-2-(piperidin-1-yl)ethanone is used as a potential anticonvulsant agent for its ability to help control and prevent seizures in patients with epilepsy or other seizure disorders.
1-(1H-indol-3-yl)-2-(piperidin-1-yl)ethanone is used as an antitumor agent for its potential to combat cancer by targeting and inhibiting tumor growth and progression.
Used in Medicinal Chemistry Research:
1-(1H-indol-3-yl)-2-(piperidin-1-yl)ethanone is used as a subject of study for its unique structure and potential biological activities, contributing to the advancement of knowledge in the field of medicinal chemistry and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 30256-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,5 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30256-73:
(7*3)+(6*0)+(5*2)+(4*5)+(3*6)+(2*7)+(1*3)=86
86 % 10 = 6
So 30256-73-6 is a valid CAS Registry Number.
30256-73-6Relevant articles and documents
QUINOLIZIDINES. IX. AN IMPROVED PROCEDURE FOR THE SYNTHESIS OF INDOLOQUINOLIZIDINE FROM 3-(2-PIPERIDINOETHYL)INDOLE
Fujii, Tozo,Ohba, Masashi,Sasaki, Noriko
, p. 1805 - 1810 (2007/10/02)
The procedure and yield of the oxidative cyclization of 3-(2-piperidinoethyl)indole (V) to produce indoloquinolizidine (X) have been improved by the use of 3 molar equivalents of Hg(OAc)2-edetate disodium in boiling aqueous EtOH for 3 h.Similar oxidation of the piperidinoethanol IIIb in boiling 1percent aqueous AcOH failed to give the expected lactam alcohol XIIb, an alternative intermediate for the synthesis of X.