New explortion of 3-Bromo-10H-phenothiazine

The design and synthesis of related molecules that are more effective, more selective, and less toxic than aspirin are important objectives of biomedical research.Keep reading other articles of 3-Bromo-10H-phenothiazine!name: 3-Bromo-10H-phenothiazine

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 3939-23-9, name is 3-Bromo-10H-phenothiazine, introducing its new discovery. name: 3-Bromo-10H-phenothiazine

Spectroscopic investigations of vinyl-substituted 10H-phenothiazine

Different 10H-phenothiazine derivatives modified at their 3- and 3,7-positions with conjugated electron-deficient pyridine or pyridinium groups using ethenyl linkers are described. Spectral variations of 3-((E)-2-(Methylpyridium-4-yl)vinyl)-10H-phenothiazine iodide and 3,7-bis((E)-2-(Methylpyridium-4-yl)vinyl)-10H-phenothiazine diiodide, which are attributed to intramolecular charge transfer, electronic rearrangement and contact ion-pair mechanisms, were observed to be either base or ion dependent. Depending on the extent of deprotonation of the nitrogen atom in the 10-position of the phenothiazine core, donor-acceptor or push-pull systems provide fluorophore-switching and potential near infrared sensor application.

The design and synthesis of related molecules that are more effective, more selective, and less toxic than aspirin are important objectives of biomedical research.Keep reading other articles of 3-Bromo-10H-phenothiazine!name: 3-Bromo-10H-phenothiazine

Reference£º
Thiazine – an overview | ScienceDirect Topics,
Thiazine | C4H5NS – PubChem