Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Research Support, U.S. Gov’t, Non-P.H.S., Journal of Organic Chemistry called Synthesis of (±)-nonactic acid, Author is Arco, Manuel J.; Trammell, Marion H.; White, James D., which mentions a compound: 3400-55-3, SMILESS is CC(Br)C(OCC)OCC, Molecular C7H15BrO2, Recommanded Product: 2-Bromopriopionaldehydediethylacetal.
(±)-Nonactic acid (I) Me ester was prepared from furan by 2 methods. 2-Lithiofuran was alkylated with propylene oxide to give alc. II which was converted in 10 further steps via tetrahydrofuryl alc. III and epinonactate IV to I Me ester. The adduct V of furan and MeCHBrCOCHBrMe was converted to I Me ester in 10 steps via alc. VI, vinyltetrahydrofuran VII, and aldehyde VIII.
From this literature《Synthesis of (±)-nonactic acid》,we know some information about this compound(3400-55-3)Recommanded Product: 2-Bromopriopionaldehydediethylacetal, but this is not all information, there are many literatures related to this compound(3400-55-3).
Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics