4370-23-4 Usage
Uses
Used in Polymer Production:
N-Vinyl-2-piperidone is used as a monomer in the production of lactam-thermoresponsive and biocompatible polymers. Its unique structure allows for the creation of polymers with temperature-sensitive properties and biocompatibility, which are essential for various applications in the medical, pharmaceutical, and biotechnology industries.
Used in Clathrate Hydrate Inhibition Research:
N-Vinyl-2-piperidone is also utilized in the study of inhibitors of clathrate hydrate formation. Clathrate hydrates are ice-like structures that can form under specific conditions and pose challenges in various industrial processes, such as oil and gas production. By studying the properties and interactions of N-vinyl-2-piperidone with clathrate hydrates, researchers can develop more effective inhibitors to prevent their formation and improve process efficiency.
Check Digit Verification of cas no
The CAS Registry Mumber 4370-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4370-23:
(6*4)+(5*3)+(4*7)+(3*0)+(2*2)+(1*3)=74
74 % 10 = 4
So 4370-23-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO/c1-2-8-6-4-3-5-7(8)9/h2H,1,3-6H2
4370-23-4Relevant academic research and scientific papers
ELECTROCHEMICAL STUDIES ON HALOAMIDES. PART VIII. ELECTROSYNTHESIS OF N-(HALO)VINYLAMIDES
Casadei, Maria Antonietta,Cesa, Stefania,Moracci, Franco Micheletti,Inesi, Achille
, p. 457 - 462 (2007/10/02)
The electrochemical reduction of N-haloethylamides 1a,b-4a,b (X = OCOCH3, Cl) at a mercury pool cathode in HCON(CH3)2 (or CH3CN) - 0.1 mol dm-3 Et4NClO4 solution has been investigated. 2,2,2-trichloroethyl derivatives 1a-4a (X = OCOCH3, Cl) give rise to the corresponding N-(2,2-dichlorovinyl)amides 5a-8a in good to excellent yields, whereas in the case of N-(2,2-dichloroethyl)amides 1b-4b the course of the reduction depends on the nature of the substituent at N-Cα and/or of the amide moiety.Acetamides 1b (X = OCOCH3, Cl) yield a mixture isomeric 5b, but pyrrolidone derivatives 2b behave differently depending on X.If X = Cl the expected isomeric dehydrohalogenation products 6b are formed, whereas vinylpyrrolidone 6c, in addition to 6b, is formed from 2b, X = OCOCH3.High yields of 6c are attained by treatment of N-(2-chloroethyl)-2-pyrrolidone, 9, with the electrogenerated pyrrolidone anion.
