Barr, Rita et al. published their research in Proceedings of the Indiana Academy of Science in 1991 | CAS: 1912-45-4

2-(5-Chloro-1H-indol-3-yl)acetic acid (cas: 1912-45-4) belongs to indole derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.Synthetic Route of C10H8ClNO2

The effect of chloro-derivatives of indoleacetic acid on plasma membrane electron transport and proton excretion was written by Barr, Rita;Boettger, Michael;Crane, Frederick L.. And the article was included in Proceedings of the Indiana Academy of Science in 1991.Synthetic Route of C10H8ClNO2 This article mentions the following:

As shown by M. Boettger and H. Hilgendorf (1988), the natural auxin indoleacetic acid in high concentrations (10 濠电偞鎸鹃幏? inhibited both e and proton efflux by corn roots of undamaged plants measured with a pH-stat combined with a redoxstat. In this study, it is shown that of various chloro-substituted indoleacetic acid derivatives, only 4-chloro-IAA inhibited NADH oxidation and several derivatives stimulated trans-membrane hexacyanoferrate reduction in concentrations from 0.1 nM to 10 濠电偞鎸鹃幏?in cultured carrot cells. Proton excretion by these cells was also stimulated by 5-, 6- and 5,7-chloro substituted indoleacetic acid, but the 4-chloro derivative inhibited H+ excretion by the plasma membrane H+-ATPase, while H+ excretion in presence of hexacyanoferrate was stimulated. These divergent effects of chloro-substituted indoleacetic acid derivatives show that the trans-membrane redox system is not directly related to proton movement through the membrane in a 1:1 relationship. In the experiment, the researchers used many compounds, for example, 2-(5-Chloro-1H-indol-3-yl)acetic acid (cas: 1912-45-4Synthetic Route of C10H8ClNO2).

2-(5-Chloro-1H-indol-3-yl)acetic acid (cas: 1912-45-4) belongs to indole derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.Synthetic Route of C10H8ClNO2

Referemce:
Indole alkaloid derivatives as building blocks of natural products from闂佽壈浜崹淇沜illus thuringiensis闂佽壈浜粋鍧闂佽壈浜崹淇沜illus velezensis闂佽壈浜粋鍧 their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles