3616-58-8 Usage
Description
N-(2,2-DIETHOXYETHYL)PIPERIDINE is a chemical compound with the molecular formula C11H23NO2. It is a versatile reagent used in various chemical reactions and processes.
Uses
Used in Chemical Synthesis:
N-(2,2-DIETHOXYETHYL)PIPERIDINE is used as a reactant for the ethylene trimerisation process, which is a chemical reaction that combines three ethylene molecules to form a propylene molecule.
Used in Pharmaceutical Industry:
N-(2,2-DIETHOXYETHYL)PIPERIDINE is used as a reactant in the synthesis of aryl-substituted piperidines. This application is crucial in the development of new pharmaceutical compounds, as aryl-substituted piperidines have potential applications in medicinal chemistry.
Used in Academic Research:
N-(2,2-DIETHOXYETHYL)PIPERIDINE is utilized in studies involving elimination reactions. These studies aim to understand the mechanisms and outcomes of elimination reactions, which are important in organic chemistry and have implications for the synthesis of various compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 3616-58-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3616-58:
(6*3)+(5*6)+(4*1)+(3*6)+(2*5)+(1*8)=88
88 % 10 = 8
So 3616-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H23NO2/c1-3-13-11(14-4-2)10-12-8-6-5-7-9-12/h11H,3-10H2,1-2H3
3616-58-8Relevant articles and documents
Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: Key precursors to potent c-Met inhibitors
Wang, Yuanxiang,Ai, Jing,Liu, Gang,Geng, Meiyu,Zhang, Ao
supporting information; scheme or table, p. 5930 - 5933 (2011/10/08)
An effective one-pot synthesis of quinolines bearing diverse C3-piperazinyl functions was developed by using a modified Friedlaender's protocol. The method not only enables the synthesis of our early reported c-Met inhibitor on a large scale, but also provides a way to generate novel multi-substituted quinolines for further structure-activity relationship (SAR) study.
