Three C-N valence vibrations in substituted dimethylanilines was written by Ritschl, Friedrich;Kuenkel, Gerhard. And the article was included in Zeitschrift fuer Physikalische Chemie (Muenchen, Germany) in 1965.Safety of 2-Chloro-N,N-dimethylaniline This article mentions the following:
The phenyl-N and the twice occurring N-methyl valence vibrations of the ir spectra were determined For the first-named kind of vibrations a linear interrelation between the Hammett substitution constants (aniline system) with a pos. slope corresponding to a decrease of the degree of bond of the phenyl-N bond was found. The other 2 frequencies, too, can be brought into a connection with the substitution constant on one hand, and with the phenyl-N valence frequency on the other hand. For the purposes of assigning of the ir spectra, the spectrum of dimethylaniline-15 N was measured. The method was applied for the determination of the constants of some substituents and the effect of an electron deficiency on the dimethylaminophenyl group in an aromatic radical mol. was determined In the experiment, the researchers used many compounds, for example, 2-Chloro-N,N-dimethylaniline (cas: 698-01-1Safety of 2-Chloro-N,N-dimethylaniline).
2-Chloro-N,N-dimethylaniline (cas: 698-01-1) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Safety of 2-Chloro-N,N-dimethylaniline
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics