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Usage

Uses

Used in Pharmaceutical Industry:
4(5H)-Thiazolone,2-(methylthio)-(9CI) is used as a potential drug candidate for its possible biological activities, which may be explored for therapeutic applications. Its unique structure could contribute to the development of new medications, pending further research and testing.
Used in Chemical Synthesis:
In the Chemical Industry, 4(5H)-Thiazolone,2-(methylthio)-(9CI) serves as an intermediate in the synthesis of other organic compounds. Its specific functional groups and ring structure make it a valuable component in creating a variety of chemical products.
The exact uses and applications of 4(5H)-Thiazolone,2-(methylthio)-(9CI) may vary and are subject to ongoing research and testing to fully understand its potential and safety in various fields.

Upstream product

• 141-84-4 2-thioxo-4-thiazolidinone 
• 74-88-4 methyl iodide 
• 34705-87-8 2-thioxothiazolidin-4-one triethylammonium salt 
• 186581-53-3 diazomethane 

Downstream Products

• 63500-79-8 2-(N-propyl-anilino)-thiazol-4-one 
• 2295-31-0 thiazoline-2,4-dione 
• 81059-99-6 2-(4-carboxy-3-hydroxyphenyl)amino-Δ²-thiazolin-4-one 
• 81059-98-5 2-(4-sulphonamidophenyl)-amino-Δ²-thiazolin-4-one 
• 19573-79-6 2-(4-oxo-thiazolidin-2-ylideneamino)benzoic acid 
• 76979-35-6 2-methylthio-5-p-chlorophenylmethylene-thiazolinone-4 
• 28996-12-5 5-(4-bromo-benzylidene)-2-methylsulfanyl-thiazol-4-one 
• 28996-52-3 2-methylsulfanyl-5-(4-nitro-benzylidene)-thiazol-4-one 
• 106992-39-6 6-[4-(4-oxo-2-thiazolin-2-ylamino)phenyl]-5-methyl-4,5-dihydro-3(2H)-pyridazinone 
• 80945-45-5 2-<4-sulphonamido-N¹-(6-methoxy-3-pyridazinyl)phenyl>amino-Δ²-thiazolin-4-one 
• 63500-78-7 2-(N-ethyl-anilino)-thiazol-4-one 
• 37394-99-3 2-(2-methyl-anilino)-thiazol-4-one 

Relevant academic research and scientific papers

Diversity-Oriented Approach to Spirorhodanines via a [2+2+2] Cyclotrimerization

Spirocyclic compounds have been increasingly utilized in drug discovery due to their inherent three-dimensional structural complexity. Here, we report a diversity oriented approach to spirorhodanines via a [2+2+2] cyclotrimerization reaction with propargyl halides as co-partners. In another sequence, we employed o-xylylene dibromide as a coupling partner to assemble spirorhodanines.