Synthesis and base strengths of some (ω-methoxyalkyl)silanes and -germanes was written by Bellama, J. M.;Gerchman, L. L.. And the article was included in Inorganic Chemistry in 1975.Category: bromides-buliding-blocks This article mentions the following:
The ethers MH3(CH2)nOMe (M = C, Si, Ge; n = 1-6) were prepared from the appropriate 1-haloalkyl methyl ethers. A comparison of their base strengths (proton affinities) as measured by the shift in the ir OH stretching frequency of MeOH on complexation with the ethers shows that some factor(s) other than inductive effects significantly influences the electron-donating ability of O in the Si and Ge hydrides when n = 1 and 2. At n = 3-6 the basicities of these ethers converge toward those of the C analogs. In the experiment, the researchers used many compounds, for example, 1-Bromo-4-methoxybutane (cas: 4457-67-4Category: bromides-buliding-blocks).
1-Bromo-4-methoxybutane (cas: 4457-67-4) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Category: bromides-buliding-blocks
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary