Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 6911-87-1, formula is C7H8BrN, Name is 4-Bromo-N-methylaniline. Organic compounds having carbon bonded to bromine are called organic bromides. SDS of cas: 6911-87-1.
Guo, Luxia;Ye, Meng;Vaccaro, Luigi;Li, Minghao;Gu, Yanlong research published ã?Two-Step Access to β-Substituted o-Hydroxyphenyl Ethyl Ketones from 4-Chromanone and its Application in Preparation of a Silica-Supported Cobalt(II) Salen Complexã? the research content is summarized as follows. A base-mediated ring opening of 4-chromanone was used to introduce the β-ethoxyl o-hydroxyphenyl Et ketone intermediary, followed by nucleophile substitution under BF3·Et2O assisted conditions to give the desired β-carbon, nitrogen, or thiol substituted o-hydroxyphenyl Et ketones I [R = p-tolyl-thiol, 1H-indol-3-yl, 2,4,5-(OMe)3C6H2, etc.; R1 = H, 5-Me, 4-OMe, etc.]. With the aid of this protocol, a silica-supported cobalt(II) salen complex was successfully prepared and its structure was confirmed by FTIR, 13C MAS NMR, UV-Vis absorption and XPS spectra. The immobilized cobalt(II) salen catalyst displayed comparable catalytic activity in the synthesis of several heterocycles including 1,3-oxazolidines II [R2 = H, F; R3 = H, Me, Cl, etc.], benzimidazole and benzoxazole as compared with their homogeneous counterparts and also could be recycled for several times without obvious loss of its catalytic activity.
SDS of cas: 6911-87-1, 4-Bromo-N-methylaniline is a aniline based compound known to exhibit mutagenic properties.
4-Bromo-N-methylaniline is a useful research compound. Its molecular formula is C7H8BrN and its molecular weight is 186.05 g/mol. The purity is usually 95%.
4-Bromophenylmethylamine is an organic compound that has anti-inflammatory properties and is used as a pharmaceutical. It belongs to the group of amines. The hydrolysis of 4-bromophenylmethylamine by hydrochloric acid produces phenol and bromamine (NHBr). The reaction system can be used to synthesize a number of compounds, including anilines, benzofurans, and other aromatic compounds. 4-Bromophenylmethylamine reacts with muscle tissue in a similar manner as acetaminophen does. This drug also has been shown to have significant effects on the energy metabolism in the muscles of rats that are given carbon source., 6911-87-1.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary