63843-57-2 Usage
Molecular Structure
1H-Indole, 3-[2-[4-(3-chlorophenoxy)-1-piperidinyl]ethyl]consists of an indole ring, a piperidine ring, and a chlorophenoxy group.
Indole Ring
A five-membered aromatic ring with a nitrogen atom at one position and a carbonyl group at the opposite position.
Piperidine Ring
A six-membered alicyclic amine containing five carbon atoms and one nitrogen atom.
Chlorophenoxy Group
A phenyl ring substituted with a chlorine atom and an ether group (-O-).
Potential Pharmaceutical Compound
This chemical compound has potential biological activity and may be used in the development of new medications.
Biological Target Interaction
The compound's structure suggests that it may interact with various biological targets, potentially leading to therapeutic effects.
Further Research
Additional studies are needed to explore the pharmacological properties and potential uses of this chemical compound to fully understand its potential.
Check Digit Verification of cas no
The CAS Registry Mumber 63843-57-2 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, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63843-57:
(7*6)+(6*3)+(5*8)+(4*4)+(3*3)+(2*5)+(1*7)=142
142 % 10 = 2
So 63843-57-2 is a valid CAS Registry Number.
63843-57-2Relevant articles and documents
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.
