Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Russian Chemical Bulletin called Salts of 2- or 3-haloalkylamines in the synthesis of N-aminoalkyl derivatives of heterocyclic and aromatic amines, Author is Vasilyeva, T. P.; Vorobyeva, D. V.; Osipov, S. N., which mentions a compound: 37481-18-8, SMILESS is NCCN1CCCC2=C1C=CC=C2, Molecular C11H16N2, SDS of cas: 37481-18-8.
Reactions of 2-haloethyl- or 3-halopropylamine salts with NH-substrates (indoline, 1,2,3,4-tetrahydroquinoline, aniline, and N-ethylaniline) in the presence of NaHCO3 in water furnished various N-aminoalkyl derivatives of heterocyclic and aromatic amines.
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Reference:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics