Name: 2-(7-Bromo-1H-indol-3-yl)acetic acid. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Response of substituted indoleacetic acids in the indolo-α-pyrone fluorescence determination. Author is Boettger, Michael; Engvild, Kjeld C.; Kaiser, Petra.
The fluorescence determination of IAA (using the fluorescence of its α-pyrone derivative) was investigated to study possible interference from 4-chloro-IAA and 5-hydroxy-IAA, which occur naturally. Both compounds showed ∼40% of the fluorescence of IAA after conversion to their α-pyrones. Halogenated IAA showed 0-60% of the fluorescence of IAA. Thus, concentration of IAA cannot be determined in crude extracts in the presence of 4-chloro- or 5-hydroxy-IAA because sep. determinations of each of these compounds are not possible by changing the excitation or fluorescence wave-lengths of the testing equipment.
In addition to the literature in the link below, there is a lot of literature about this compound(2-(7-Bromo-1H-indol-3-yl)acetic acid)Name: 2-(7-Bromo-1H-indol-3-yl)acetic acid, illustrating the importance and wide applicability of this compound(63352-97-6).
Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com