62114-70-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(chloromethyl)-1-methyl-4-phenylpiperidine serves as a starting material for the synthesis of various pharmaceuticals, contributing to the development of novel drug candidates due to its unique structural features.
Used in Organic Chemistry Research:
2-(chloromethyl)-1-methyl-4-phenylpiperidine is utilized as a reagent in the preparation of complex organic molecules, particularly in research laboratories, where its properties are harnessed to advance scientific understanding and innovation in organic chemistry.
Used in Chemical Synthesis:
2-(chloromethyl)-1-methyl-4-phenylpiperidine is employed as a building block in the synthesis of a range of organic compounds, highlighting its importance in the creation of diverse chemical entities for various applications.
Safety Note:
Given its potentially hazardous nature, 2-(chloromethyl)-1-methyl-4-phenylpiperidine should be handled with caution, and strict adherence to safety protocols is essential when working with 2-(chloromethyl)-1-methyl-4-phenylpiperidine in any capacity.
Check Digit Verification of cas no
The CAS Registry Mumber 62114-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,1 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62114-70:
(7*6)+(6*2)+(5*1)+(4*1)+(3*4)+(2*7)+(1*0)=89
89 % 10 = 9
So 62114-70-9 is a valid CAS Registry Number.
62114-70-9Relevant academic research and scientific papers
SYNTHESE RADICALAIRE D'ANALGESIQUES POTENTIELS: ARYL-4 PIPERIDINES SUBSTITUEES EN 2 ET BENZOMORPHANES
Stella, L.,Raynier, B.,Surzur, J. M.
, p. 2843 - 2854 (2007/10/02)
The synthesis of a series of 3-aryl 5-hexenyl amines and the cyclisations of the corresponding N-chloroamines are described.When the ring closure results from the amino radical addition to the ethylenic double bond, 2-chloromethyl 4-phenyl piperidines are obtained.These compounds lead by intramolecular Friedel-Crafts reaction to varied substituted 6,7-benzomorphanes.When the phenyl ring is substituted with a methoxyl group, the cyclisation proceeds via homolytic aromatic substitution and 4-allyl tetrahydroquinolines are formed.
