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, 89-63-4, Name is 4-Chloro-2-nitroaniline, SMILES is NC1=CC=C(Cl)C=C1[N+]([O-])=O, in an article , author is Letessier, Julien, once mentioned of 89-63-4, Computed Properties of C6H5ClN2O2.
Synthesis of a Naphtho-pyrido-Annulated Iodonium Salt and Pd-Catalyzed Transformation to 7H-Naphtho[1,8-bc][1,5]naphthyridine
Nitropyridylnaphthalene is the central intermediate for the synthesis of naphthonaphthyridine and benzo–carboline. Whereas the Cadogan reaction gives the carboline, transformation of the nitro group to iodo followed by oxidation and cyclization results in an iodonium salt. A twofold Pd-catalyzed amination leads to the naphthyridine.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 89-63-4, you can contact me at any time and look forward to more communication. Computed Properties of C6H5ClN2O2.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem