Safety 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 Preparation of chlorinated 3-indolylacetic acids. Author is Engvild, K. C..
Indoleacetic acids I (Rn = 4-Cl, 6-Cl) were prepared in 38-40% yield by reaction of the resp. chloro(diethylaminomethyl)indole with NaCN followed by hydrolysis. I (Rn = 5-Cl, 7-Cl, 4,6-Cl2, 4,7-Cl2, 5,7-Cl2, 6,7-Cl2, 5-Cl-7-Me, 7-Br) were prepared in 7-28% yield by reaction of HCOCH2CH2CO2H with the appropriate phenylhydrazine hydrochlorides.
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Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com