63843-67-4 Usage
Chemical structure
1H-Indole, 3-[2-[4-(4-fluorophenoxy)-1-piperidinyl]ethyl]-2-methylis a complex organic compound consisting of an indole ring, a piperidine ring, a fluorophenoxy group, and a methyl group.
Indole ring
A heterocyclic aromatic ring system with a five-membered carbon ring and a six-membered nitrogen-containing ring.
Piperidine ring
A six-membered heterocyclic amine ring system with the structure of a saturated azacyclohexane.
Fluorophenoxy group
A structural group consisting of a phenyl ring (a six-membered carbon ring with alternating single and double bonds) connected to an oxygen atom, with one of the hydrogen atoms on the phenyl ring replaced by a fluorine atom.
Methyl group
A hydrocarbon group with one carbon atom bonded to three hydrogen atoms (-CH3).
Pharmaceutical applications
The compound may have potential pharmaceutical applications due to the presence of biologically active substructures, such as the indole and piperidine rings.
Pharmacological properties
The presence of the fluorophenoxy group could influence the compound's pharmacological properties, such as its activity, potency, and selectivity.
Further research
Additional research and investigation are needed to fully understand the potential uses and effects of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 63843-67-4 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, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63843-67:
(7*6)+(6*3)+(5*8)+(4*4)+(3*3)+(2*6)+(1*7)=144
144 % 10 = 4
So 63843-67-4 is a valid CAS Registry Number.
63843-67-4Relevant 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.
