Design and characterization of some new non-symmetric substituted triazines and triazine derivatives was written by Thakare, S. S.;Dhote, S. N.. And the article was included in International Journal of Pharmaceutical Sciences and Research in 2020.Category: chlorides-buliding-blocks The following contents are mentioned in the article:
Attempts were made to carry out the laboratory synthesis of non-sym. mono-, di- and tri- substituted 1,3,5-triazines I (R = Et, Ph, 2,5-dimethylphenyl, 4-nitrophenyl, etc.; R1 = Cl, naphthalen-1-oxy; R2 = Cl, benzothiazol-2-ylsulfanyl, phenylsulfanyl) by the action of the electron-donating substituent on 2,4,6-trichloro-1,3,5-triazine by aromatic nucleophilic substitution reaction mechanism (SNAr reaction) by temperature controlled. The introduction of the amino group (-NH-), ether (-O-) and thiol (-S-) Linker Bridge show more promising antibacterial activity. The yield of newly synthesized compounds I was quite well, and their structures were confirmed by using IR, 1H NMR, and Mass spectral data. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Category: chlorides-buliding-blocks).
4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Category: chlorides-buliding-blocks
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics