136704-10-4 Usage
Uses
Used in Pharmaceutical Synthesis:
1-benzyl-4-(chloromethyl)piperidine(SALTDATA: HCl) is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with potential therapeutic applications.
Used in Organic Chemistry:
As a building block in organic chemistry, 1-benzyl-4-(chloromethyl)piperidine(SALTDATA: HCl) is utilized for the creation of diverse organic compounds, leveraging its unique structural features to form novel molecules with specific properties and potential applications.
Used in Medicinal Chemistry Research:
1-benzyl-4-(chloromethyl)piperidine(SALTDATA: HCl) is employed as a compound of interest in medicinal chemistry research, where its potential pharmacological properties are explored for the development of new therapeutic agents and the enhancement of existing ones.
The physical and chemical properties of 1-benzyl-4-(chloromethyl)piperidine(SALTDATA: HCl), along with its potential uses, make it a valuable compound for further study and development in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 136704-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,0 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136704-10:
(8*1)+(7*3)+(6*6)+(5*7)+(4*0)+(3*4)+(2*1)+(1*0)=114
114 % 10 = 4
So 136704-10-4 is a valid CAS Registry Number.
136704-10-4Relevant academic research and scientific papers
Convenient preparation of aryl ether derivatives using a sequence of functionalized polymers
Lizarzaburu, Mike E.,Shuttleworth, Stephen J.
, p. 4873 - 4876 (2007/10/03)
A four-step synthesis to aryl ether derivatives, three of which utilize polymer-supported reagents, has been developed. Supported triphenylphosphine was successfully utilized in two distinct synthetic processes in the first step, whilst supported base and ionic and covalent scavengers were employed to complete the synthesis and purification of the target compounds.
