Application In Synthesis of 2-(7-Bromo-1H-indol-3-yl)acetic acid. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 2-(7-Bromo-1H-indol-3-yl)acetic acid, is researched, Molecular C10H8BrNO2, CAS is 63352-97-6, about Substituted indoleacetic acids tested in tissue cultures. Author is Engvild, Kjeld C..
Monochloro substituted indole-3-acetic acids inhibited shoot induction in tobacco tissue cultures about as much as IAA. Dichloro substituted indole-3-acetic acids inhibited shoot formation less. Other substituted indoleacetic acids except 5-fluoro- and 5-bromoindole-3-acetic acid were less active than IAA. Callus growth was quite variable and not correlated with auxin strength measured in the Avena coleoptile test.
In some applications, this compound(63352-97-6)Application In Synthesis of 2-(7-Bromo-1H-indol-3-yl)acetic acid is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com