Relation between electronic structure and auxin activity of chlorinated β-indolylacetic acids was written by Cocordano, Maurice;D’Amato, Franck;Turcat, Jean J.. And the article was included in Annales de la Faculte des Sciences de Marseille in 1970.Recommanded Product: 1912-45-4 This article mentions the following:
Five chlorinated β-indolylacetic acids (I) were prepared by the cyclization of ClC6H4NHN:CHCH2CH2CO2H in ethanolic H2SO4 followed by saponification The auxinic activity of I derivatives was in the order 6-Cl- > nonchlorinated > 6,7-Cl2 > 7-Cl > 5,7-Cl2. The electronic structure of I was calculated by LCAO method. I forms by, its CO2H group, a conjugated unstable complex with the protein of the cell. In the experiment, the researchers used many compounds, for example, 2-(5-Chloro-1H-indol-3-yl)acetic acid (cas: 1912-45-4Recommanded Product: 1912-45-4).
2-(5-Chloro-1H-indol-3-yl)acetic acid (cas: 1912-45-4) belongs to indole derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. Due to this activity, the indole ring system has become an important component or intermediate in the synthesis of heterocycles.Recommanded Product: 1912-45-4
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles