Dual Functional Salts of Benzo[1.2.3]thiadiazole-7-carboxylates as a Highly Efficient Weapon Against Viral Plant Diseases was written by Smiglak, Marcin;Lewandowski, Piotr;Kukawka, Rafal;Budziszewska, Marta;Krawczyk, Krzysztof;Obrepalska-Steplowska, Aleksandra;Pospieszny, Henryk. And the article was included in ACS Sustainable Chemistry & Engineering in 2017.Recommanded Product: 1-Dodecylpyridin-1-ium bromide This article mentions the following:
Nowadays, plant protection against viral diseases is one of the most challenging tasks faced by modern agriculture. One of the possible ways of plant protection is utilization of systemic acquired resistance phenomenon. In this approach biol. or chem. factors interact with plants and stimulate their immune system against infections before infection occurs. This paper presents 11 ionic derivatives of benzo[1.2.3]thiadiazole-7-carboxy-S-Me ester, a synthetic plant resistance inducer, with counterions specifically selected to modify the phys. and biol. properties of the resulting salts. We present the synthesis methods, as well as phys. and biol. properties, of these newly obtained anionic bifunctional salts. In the experiment, the researchers used many compounds, for example, 1-Dodecylpyridin-1-ium bromide (cas: 104-73-4Recommanded Product: 1-Dodecylpyridin-1-ium bromide).
1-Dodecylpyridin-1-ium bromide (cas: 104-73-4) belongs to pyridine derivatives. The ring atoms in the pyridine molecule are sp2-hybridized. The nitrogen is involved in the π-bonding aromatic system using its unhybridized p orbital. The lone pair is in an sp2 orbital, projecting outward from the ring in the same plane as the σ bonds. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Recommanded Product: 1-Dodecylpyridin-1-ium bromide