16682-30-7

Upstream product

• 137-07-5 2-amino-benzenethiol 
• 16452-09-8 (2-aminophenyl)-4’-methylphenyl sulfide 
• 92740-87-9 10-(p-tolyl)-10H-phenothiazine 
• 92-84-2 10H-phenothiazine 
• 624-31-7 4-tolyl iodide 

Relevant academic research and scientific papers

Transition-Metal-Free Synthesis of N-Arylphenothiazines through an N- And S-Arylation Sequence

An efficient synthetic method of N-arylphenothiazines from o-sulfanylanilines under transition-metal-free conditions is disclosed. An N- and S-arylation sequence of o-sulfanylanilines enabled us to synthesize a wide variety of N-arylphenothiazines. In par

Room temperature phosphorescence molecule based on phenothiazine derivative, preparation method and application thereof

The invention discloses a room temperature phosphorescence molecule based on a phenothiazine derivative, a preparation method and application thereof. The room temperature phosphorescence molecule based on the phenothiazine derivative has a structure shown as formula (I), wherein R is -OCH3, -CH3, -H, -Br, -Cl, -F or -CF3. According to the invention, mainly phenothiazine is adopted as the core, and C-N coupling reaction is carried out to connect phenothiazine with a benzene ring derivative, and then oxidation is carried out to obtain the target product. The solid powder of the compounds all have room temperature phosphorescence phenomenon, and have a longest life up to 398ms, thus being applicable as anti-counterfeit materials. And the preparation method provided by the invention has the advantages of mild reaction conditions and high yield.