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, Organometallics called The anomalous electrochemistry of the ferrocenylamines, Author is Britton, Wayne E.; Kashyap, Ram; El-Hashash, Maher; El-Kady, Mohammed; Herberhold, Max, which mentions a compound: 1273-73-0, SMILESS is Br[C-]12[Fe+2]3456789([C-]%10C6=C7C8=C9%10)C1=C3C4=C25, Molecular C10BrFe, COA of Formula: C10BrFe.
In the electrochem. of ferrocenylamines, the amine substituent acts as an unusually potent activating group for ferrocene oxidation, as shown by various Hammett-type correlations, with ferrocenylamine oxidizing at a potential 0.37 V more neg. than ferrocene itself. Triferrocenylamine, a compound with a nearly planar N, produces three reversible oxidation waves, the first of which is 0.31 neg. of ferrocene’s oxidation These and other data suggest that resonance interaction between ferrocene and the N lone pair is an important factor in ferrocene oxidation This contrasts with conclusions of earlier studies in which ferrocenes, with primarily electron-withdrawing groups, were examined
From this literature《The anomalous electrochemistry of the ferrocenylamines》,we know some information about this compound(1273-73-0)COA of Formula: C10BrFe, but this is not all information, there are many literatures related to this compound(1273-73-0).
Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com