33284-28-5

Usage

Uses

Used in Organic Synthesis:
3-(Dimethylamino)benzenethiol is used as a building block in organic synthesis for the preparation of various chemical products. Its unique structure allows it to be a key component in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
3-(Dimethylamino)benzenethiol is used as an intermediate in the development of pharmaceuticals, particularly for anti-inflammatory and anti-cancer drugs. Its antioxidant properties and potential therapeutic effects make it a valuable asset in medicinal chemistry.
Used in Dye Industry:
In the dye industry, 3-(Dimethylamino)benzenethiol is utilized for the production of dyes due to its chemical structure that can impart color to various materials.
Used in Fragrance Industry:
3-(Dimethylamino)benzenethiol is used as a scent additive in perfumes and other fragrances, capitalizing on its naturally strong odor to enhance or create unique scents in a variety of products.

Upstream product

• 925-89-3 Prop-1-en-1-thiol 
• 16518-62-0 3-bromo-N,N-dimethylaniline 

Downstream Products

• 705964-31-4 bis-3-(N,N-dimethylamino)phenyldisulfide 
• 923583-92-0 N,N-dimethyl-3-(3-(1-methyl-1H-pyrazol-4-yl)-1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrrolo[2,3-b]pyridin-5-ylthio)aniline 
• 705964-32-5 N,N-Diethyl 4-N,N-Dimethylamino-2-[3-(N,N-dimethylamino)-phenylthio]benzamide 

Relevant academic research and scientific papers

Aminothioxanthone Derivatives

The present invention refers to 350 to 400 nm range of zero increase/decrease high absorbance of photocurable composition in use can be transporting, a light in an ultraviolet range by the irradiation of electromagnetic waves of fluorescent greater efficiency high efficiency that is capable of emitting light, the aminosilane is fluorescent materials reliability thioxanthone derivative.

Novel chalcogenoxanthylium dyes for purging blood pathogens and for photodynamic therapy

Provided are chalcogenoxanthylium compounds which can effectively be used as sensitizers in photodynamic therapy, virucides in photodynamic antimicrobial chemotherapy and reversal agents of Pgp function in cancer cells. Further provided is a general metho

Synthesis, properties, and photodynamic properties in vitro of heavy-chalcogen analogues of tetramethylrosamine

Thio and seleno analogues of tetramethylrosamine were prepared by the directed-metalation/cyclization of the corresponding N,N-diethyl 2-(3-dimethylaminophenylchalcogeno)-4-dimethylaminobenzamide to the 2,7-bis-(N,N-dimethylamino)-9H-chalcogenoxanthen-9-one followed by the addition of phenylmagnesium bromide, dehydration, and ion exchange to the chloride salt. The thio and seleno tetramethylrosamines had longer wavelengths of absorption and higher quantum yields for the generation of singlet oxygen than tetramethylrosamine. Both the thio and selenoanalogues of tetramethylrosamine were efficient photosensitizers against R3230AC rat mammary adenocarcinoma cells in vitro.