14204-35-4

Basic information

• Product Name: 5,5-Dimethyl-3-phenylthiohydantoin
• Synonyms: 5,5-Dimethyl-3-phenylthiohydantoin
• CAS NO: 14204-35-4
• Molecular Weight: 236.294
• Mol File: 14204-35-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5,5-Dimethyl-3-phenylthiohydantoin(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-Dimethyl-3-phenylthiohydantoin(14204-35-4)
• EPA Substance Registry System: 5,5-Dimethyl-3-phenylthiohydantoin(14204-35-4)

Safety Data

• Hazardous Substances Data: 14204-35-4(Hazardous Substances Data)

Upstream product

• 77-71-4 5,5-dimethyl-imidazolidine-2,4-dione 
• 931-59-9 benzenesulfenyl chloride 

Downstream Products

• 29959-86-2 1-(phenylsulphenyl)piperidylamide 
• 4837-31-4 4-Phenylsulfanyl-morpholine 
• 7257-54-7 1,4-bis-phenylsulfanyl-piperazine 
• 5285-87-0 phenyl thiocyanate 
• 128070-46-2 5,5-dimethyl-1-phenylsulfanyl-imidazolidine-2,4-dione 
• 128070-50-8 2-(phenyldisulfanyl)benzo[d]thiazole 
• 14933-91-6 N-phenyl-benzenesulphenamide 
• 128070-43-9 3,5,5-Trimethyl-1-phenylsulfanyl-imidazolidine-2,4-dione 

Relevant articles and documents

In Search of New Sulfur Transfer Agents

The chemistry of various sulfur-transfer agents is studied.The reaction of aromatic sulfenyl chloride 5 in the presence of imidazole and/or triethylamine gives the aryl disulfides 7 in 14-85 percent yield, whereas in the case of the corresponding benzylsulfenyl chlorides 9 in the presence of triethylamine and/or caprolactam, both disulfide 10 and benzyl chlorides 11 are formed in 0-81 precent and 10-72 precent yield, respectively. - The transfer reactions of 3-sulfenylated hydantoins 18 with amines are useful for the preparation of the unsymmetric sulfenamides 20 in 31 -61 percent yield.Analogous transfer reactions of compounds 23 and 24 with piperidine give N,N'-thiodipiperidine (3, X = CH2) in 71-80 percent.