63843-73-2 Usage
Indole ring
A five-membered aromatic ring with a nitrogen atom at one position, contributing to the compound's aromaticity and potential pharmacological activity.
Methoxy groups (two)
Oxygen atoms bonded to a methyl group (-OCH3), attached to the indole ring's carbon atoms at positions 5 and 6, increasing the compound's polarity and solubility.
Ethyl group
A two-carbon chain (-CH2-CH3), attached to the oxygen atom of the methoxy group at position 6, increasing the compound's molecular weight and size.
Piperidine ring
A five-membered nitrogen-containing ring (N-C5H4), bonded to the ethyl group, contributing to the compound's structural complexity and potential biological activity.
Trifluoromethyl group
A carbon atom bonded to three fluorine atoms (-CF3), attached to the phenyl ring of the phenoxy group, increasing the electronegativity and lipophilicity of the compound.
Phenoxy group
A phenyl ring (C6H5) bonded to an oxygen atom (-C6H4-O), attached to the piperidine ring, contributing to the compound's aromaticity and potential pharmacological activity.
Potential pharmacological and biological activities
The diverse molecular composition, including various functional groups and structural features, may contribute to the compound's ability to interact with biological targets, making it of interest for further study and investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 63843-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,4 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63843-73:
(7*6)+(6*3)+(5*8)+(4*4)+(3*3)+(2*7)+(1*3)=142
142 % 10 = 2
So 63843-73-2 is a valid CAS Registry Number.
63843-73-2Relevant academic research and scientific papers
Piperidylalkylindoles. 1. Hypotensive activity of 3-[2-(phenoxypiperidyl)ethyl]indoles
Helsley,Strupczewski,Woodward
, p. 309 - 312 (2007/10/05)
A series of 3-[2-(phenoxypiperidyl)ethyl]indoles was synthesized and evaluated for hypotensive activity in the spontaneous hypertensive rat. Maximum hypotensive activity appeared when the phenoxy substituent was para substituted and occupied the 4 position of the piperidine ring.
Method of treating pain and hypertension
-
, (2008/06/13)
3-[2-(Phenyloxycycloazalkyl)ethyl]indoles possessing antihypertensive, analgesic, and tranquilizing properties and process for their preparation are described.
