96963-72-3

Upstream product

• 106-43-4 para-chlorotoluene 
• 134-32-7 1-amino-naphthalene 
• 104-86-9 4-chlorobenzylamine 
• 96963-41-6 4-Chloro-N-naphthalen-1-yl-thiobenzamide 
• 28353-74-4 3,4-dihydronaphthalen-1(2H)-one O-acetyl oxime 
• 104-88-1 4-chlorobenzaldehyde 
• 96963-52-9 4-chloro-N-(naphthalen-1-yl)benzamide 

Relevant academic research and scientific papers

Graphene oxide-catalyzed synthesis of benzothiazoles with amines and elemental sulfur via oxidative coupling strategy of amines to imines

The graphene oxide-catalyzed coupling and cyclization reactions of primary amines with elemental sulfur was developed to afford various optically property benzothiazoles. This coupling and cyclization strategies proceeded under the oxidant system graphene oxide/O2 and constructed carbon-heteroatom (N, S) bonds with amines and elemental sulfur. Due to benzothiazoles as common chromophores, these products exhibited intriguing fluorescence properties, including outstanding Stokes shifts (up to 161 nm) and quantum yields (up to 74%). Utilizing the products’ unique fluorescence response in different solvents, β-naphthothiazole 4a showed excellent aggregation-induced emission properties in 1,2-dichloroethane, which was 60 times higher than in tetrahydrofuran.

Multi-substituted naphtho[1,2-d]thiazole and derivatives and synthesis method thereof

The invention relates to multi-substituted naphtho[1,2-d]thiazole and derivatives and a synthesis method thereof. For the first time, ketoxime ester compounds, formaldehyde compounds and sulfur powderare converted into multi-substituted naphtho[1,2-d]thia