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Although many compounds look similar to this compound(1273-73-0)Reference of Bromoferrocene, numerous studies have shown that this compound(SMILES:Br[C-]12[Fe+2]3456789([C-]%10C6=C7C8=C9%10)C1=C3C4=C25), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Action of halogens on ferrocenylgold-triphenylphosphine, published in 1971, which mentions a compound: 1273-73-0, mainly applied to ferrocenyl gold phosphine bromination, Reference of Bromoferrocene.

Ph3P.AuC5H4FeC5H5 (I) brominated in CCl4 at -20° to a blue, then yellow material and after evaporation gave 55% bromoferrocene and 18% biferrocenyl along with 70% Ph3P.AuBr. Similar results were obtained at -50° in CH2Cl2. I chlorinated as above to 26% chloroferrocene, 70% biferrocenyl, and 98% Ph3P.AuCl. Iodination gave 82% iodoferrocene and 89% Ph3P.AuI.

Although many compounds look similar to this compound(1273-73-0)Reference of Bromoferrocene, numerous studies have shown that this compound(SMILES:Br[C-]12[Fe+2]3456789([C-]%10C6=C7C8=C9%10)C1=C3C4=C25), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com