52900-93-3 Usage
Description
(E)-alpha-ethylidenepiperidine-1-acetaldehyde, also known as 1-acetyl-4-ethylpiperidine, is a chemical compound with the molecular formula C11H17NO. It is a derivative of piperidine, a heterocyclic amine, and is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. This colorless liquid at room temperature has a sharp, pungent odor and is soluble in most organic solvents. Its potential use in the field of organic synthesis and chemical research makes it a valuable compound for further development and application.
Uses
Used in Pharmaceutical Industry:
(E)-alpha-ethylidenepiperidine-1-acetaldehyde is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of a wide range of medicinal compounds.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-alpha-ethylidenepiperidine-1-acetaldehyde is used as a key compound for the production of various chemicals and materials. Its versatility in reacting with other substances makes it a valuable asset in creating a diverse array of products.
Used in Chemical Research:
(E)-alpha-ethylidenepiperidine-1-acetaldehyde is also utilized in chemical research as a subject for studying the properties and reactions of heterocyclic amines. This helps in understanding the behavior of similar compounds and contributes to the advancement of chemical knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 52900-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,0 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52900-93:
(7*5)+(6*2)+(5*9)+(4*0)+(3*0)+(2*9)+(1*3)=113
113 % 10 = 3
So 52900-93-3 is a valid CAS Registry Number.
52900-93-3Relevant articles and documents
Multistep nucleophilic substitution of the halogen atom in 2-halo-2-alkenals
Rulev,Zinchenko,Keiko,Voronkov
, p. 129 - 132 (2007/10/03)
ipso-Substitution of the halogen atom in 2-halo-2-alkenals under the action of secondary amines proceeds via three consecutive steps: addition, nucleophilic substitution, and β-elimination (the AdN-SN-E mechanism). The main intermediates arising in the reactions of 2-chloropropenal and 2-chloro-2-butenal with piperidine were detected by NMR spectroscopy. A general scheme of the reaction is proposed.
