Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 461432-23-5, Name is 4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene, SMILES is CCOC1=CC=C(CC2=C(Cl)C=CC(Br)=C2)C=C1, in an article , author is Akbari, Mosayeb, once mentioned of 461432-23-5, Safety of 4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene.
An efficient method is applied for the synthesis of novel 2-(2-chloroquinolin-3-yl)-N-alkylimidazo[1,2-a]pyridin-3-amine derivatives. The method is based on a two-step approach from acetanilide, 2-chloro-3-formyl quinoline, 2-aminopyridine, and isocyanide under mild reaction conditions. In the first step, acetanilide forms 2-chloroquinoline-3-carbaldehyde in the presence of phosphoryl chloride. The synthesized 2-chloroquinoline-3-carbaldehyde takes part in a multicomponent reaction with 2-aminopyridine, and isocyanide in the presence of trimethylsilyl chloride. The reaction is facile and the products are synthesized in high isolated yields under mild reaction conditions.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 461432-23-5, you can contact me at any time and look forward to more communication. Safety of 4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene.
Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics