63843-49-2 Usage
General Description
4-(4-Methylphenoxy)Piperidine Hydrochloride is a synthetic chemical compound classified as an organic compound. It is primarily an intermediate used in the production of other advanced chemical compounds in a variety of industries from pharmaceuticals to performance materials. 4-(4-METHYLPHENOXY)PIPERIDINE HYDROCHLORIDE has a complex structure, including methyl and hydrochloride components, and a carbon-rich phenyl group attached to a piperidine ring. The compound's properties, such as its solubility and reactivity, along with its potential hazards and handling instructions, may vary based on its concentration and the other chemicals with which it is combined.
Check Digit Verification of cas no
The CAS Registry Mumber 63843-49-2 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, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63843-49:
(7*6)+(6*3)+(5*8)+(4*4)+(3*3)+(2*4)+(1*9)=142
142 % 10 = 2
So 63843-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-10-2-4-11(5-3-10)14-12-6-8-13-9-7-12/h2-5,12-13H,6-9H2,1H3
63843-49-2Relevant articles and documents
N- versus O-arylation of aminoalcohols: Orthogonal selectivity in copper-based catalysts
Shafir, Alexandr,Lichtor, Phillip A.,Buchwald, Stephen L.
, p. 3490 - 3491 (2008/01/01)
Two complementary protocols for copper-catalyzed arylation of aminoalcohols were developed. Selective N-arylation was accomplished at room temperature using 2-isobutyrylcyclohexanone (a β-diketone) as supporting ligand, while selective O-arylation require
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.
