Our Top Choice Compound: 57825-30-6

Here is just a brief introduction to this compound(57825-30-6)Application In Synthesis of 1-(Bromomethyl)-4-ethylbenzene, more information about the compound(1-(Bromomethyl)-4-ethylbenzene) is in the article, you can click the link below.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Polymer-supported reagents: polar effects in substrate selectivity, published in 1982-07-01, which mentions a compound: 57825-30-6, Name is 1-(Bromomethyl)-4-ethylbenzene, Molecular C9H11Br, Application In Synthesis of 1-(Bromomethyl)-4-ethylbenzene.

A selectivity effect was observed in the competitive reaction of a polymer-supported nucleophile with pairs of halides of analogous size but different polarity. Competitive esterification with Amberlyst A-26 (AcO-) of Br(CH2)4CO2Et and Me(CH2)7Br showed a marked preference for the halide with a polar tail, the relative rates being 1.9 and 1.0, resp.

Here is just a brief introduction to this compound(57825-30-6)Application In Synthesis of 1-(Bromomethyl)-4-ethylbenzene, more information about the compound(1-(Bromomethyl)-4-ethylbenzene) is in the article, you can click the link below.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider